Органические реакции, Сборник 14 - Коп А.
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Литература (выход, %)
I
(C6H5CONHCHCHCi2J2O
208
C6H5CONHCH(OCH3)CHBr2
208
I
(C6H5CONHCHCHBr2)20
208
C6H5CONHCH(OCh3)CCI3
95
C6H5CONHCH(OC2H5)CCi3
95
I
(C6H5CONHCHCCIg)2O
95, 229
C6H5CONHCH(OCH3)CBr3
166
I
(C6H5CONHCHCBr3)20
166
C6H5CONHC(OC2H5)(C6H5).,
231
QH5CONHC(OC4H9-«)(C6H5)2
231
2-HO-S1S-Br2C6H2CONHCH(OCH3)CCl3
228
2-HO-3-02NC6H3CONHCH(OCH3)CCl3
225
2-HO-5-Br-3-02NC6H2CONHCH(OCH3)CCl3
225
2-HO-3,5-(02N)2C6H2CONHCH(OCHg)CCl3
225
2-CH3OC6H4CONHCH(OCH3)CBr3
166
J
(2-CH3OC6H4CONHCHCBr3J2O
166
2-CH30-3-ClC6H3CONHCH(OCH3)CCl3
226
2-CH30-5-ClC6H3CONHCH(OCH3)CCl3
206, 226
2-CH30-5-ClC6H3CONHCH(OC2H5)CCl3
206
2-CH30-5-ClC6H3CONHCH(OC6H5)CClg
206
j
(2-CH30-5-ClC6H3CONHCHCCl3)20
226
2-CH3O-S1S-CI2C6H2CONHCH(OCh3)CCI3
206, 226
2-CH30-3,5-Cl2C6H2CONHCH(OC6H5)CCl3
206
j
(2-CH30-3,5-Cl2C6H2CONHCHCCl3)20
226
2-CH3O-S-BrC6H3CONHCH(OCH3)CCl3
228
2-CH30-5-BrC6H3CONHCH(OC2H5)CCl3
205
2-CH30-5-BrC6H3CONHCH(OC6H5)CCl3
205
j
(2-CH3O-S-BrC6H3CONHCHCCIg)2O
228
2-CH3O-S1S-Br2CeH2CONHCH(OCH3)CCl3
228
(2-CH30-3,5-Br2C6H2CONHCHCCl3)20
228
2-CH30-3-02NC6H3CONHCH(OCH3)CCl3
і
205, 225
Продолжение табл. 25
Простые эфиры N-cc-оксналкильных производных
Литература (выход, %)
I
(2-CH30-3-02NCeH3CONHCHCCl3)20
2-CH30-5-02nceH3CONHCH(OCH3)CCl3
2-CH3O-s-O2NCeH3CONHCH(OC2H5)CCl3
225
205, 225 205
j
(2-CH30-5-02NCeH3CONHCHCCl3)20 0-CH3C6H4CONHCH(OCh3)CCI3 0-CH3C6H4CONHCH(OC2H5)CCi3 0-CH3C6H4CONHCH(Oc6H5)CCI3
225
106, 168
106
106
I
(o-CH3CeH4CONHCHCCl3)20
A-CH3C6H4CONHCH(OCh3)CCI3
A-CH3C6H4CONHCH(OC2H5)CCi3
X-CH3C6H4CONHCH(Oc6H5)CCI3
X-CH3C6H4CONHCH(Cc6H4CH3-O)CCI3
168 106 106 106 106
I
(ж-сНзС6н4ажнснссі3)2о
n-CH3C6H4CONHCH(OCH3)CCl3
H-CH3C6H4CONHCH(OC2H5)CCi3
,1-CH3C0H4CONHCH(OCeH5)CCl3
168 106 106 106
I
(n-CH3C6H4CONHCHCCl3)20
Ii ii
168 •i... ¦
I4 J-CONHCH(OCh3)CCI3
O
204(80)
I]4 J— CONhCH(OC2H5)CCI3 O
204 (70)
Br—I| y— CONHCH(OCh3)CCI3 O
204 (92)
O2N —CONHCH(OCh3)CCI3 O
204 (57)
(CH3J3C—I J-CONHCH(OCh3)CCI3 O
204 (100)
214
Продолжение табл. 25
Простые эфиры N-a-оксиалкильных производных
Литература (выход, %)
Лактамы и имиды CH2CO •
I 4NCH(OCH3)CCl3
СН2СН2
CH2CO
I 4NCH(OC2H5)CH3 ;
CH2CO
CH2GO
j 4NCH(OC4H9-W)CH3 (
CH2CO
CH2CO
I 4NCH(OC6H5)CH3
CH2CO
CH2CO
H2C^ 4NCH(OC4H9-H)CH3 CH2CO
0-C6H4(CO)2NCH(OC2H5)CH3 0-C6H4(CO)2NCH(OC6H5)CH3 0-C6H4(CO)2NCH(OC2H5)CH2Br
Карбамильные соединения CH3O2CNHCH(OCh3)CCI3
I
(CH302CNHCHCC13)20 C2H5O2CNHCH(OC4H9-H)CH3 C2H5O2CNHCH(OCH3)CCi3 C2H5O2CNHCH(OC2H5)CCl3
(C2H502CNHCHCCl3)20
C2H5O2CNHCH(OCH2CH = CH2)CH(NHCO2C2H5J2 C2H5O2CNHCH(OCh2C6H5)CH(NHCO2C2H5J2
I
(C2H5O2CNHCHOCH3J2 C2H5O2CN(CH3)CH(OCH3)C6H5 H-C4H9O2CNHCH(OC2H5)CHi(NHCO2C4H9-H)2 I
(«30-C5H11O2CNHCHCCIg)2O 1-C10H7O2CNHCH(OCh3)CCI3
101 (50)
232 (93)
232 (95)
232 (79)
232 (91)
232 (82) 232 (41) 214 (63)
73, 95 95
234 (79)
94
94
94, 95, 229, 230
223
223
223
216(62)
223 (хороший)
95 73
215
Продолжение табл. 25
Простые эфнры N-Cfc-оксналкильных производных
Литература (выход, X)
2-Ci0H7O2CNHCH(OCH3)CdI3
H2NCONHCH(OCH3)CCi3
H2NCONHCH(OC2H5)CCi3
H2NCONHCH(OC3H7-H)CCi3
H9NCONHCH(OC4H9-H)CCIi
І і
(H2NC0NHCHCC13)20 J H2NCONHCH(OCH3)CBr3 ; H2NCONHCH(OC2H5)CBr3 [ HKNCONHCH(OC3H7-H)CBr3
(H2NCONHCHCBr3)20
(ClNHCONClCHCCl3)20 !
I •
¦CH3NHCONHCH(OC2H5)CCI3
I j
(CH3NHC0NHCHCC13)20 ,
CH3NHCONHCH(OC2H5)CBJr3
(CH3NHCONHCHCBr3)20 j C2H5NHCONHCH(OCH3)CCiI3 C2H5NHCONHCH(OC2H5)Cq3 C2H5NHCONHCH(OCsH7-H)CCI3 C2H5NHCONHCH(OC4H9-H)CCi3 I
(C2H5NHCONHCHCCl3)20 '-
CeH5NHCONHCH(OC4H97H)CH3
CBH5NHCONHCH(OCH3)COs
CeH5NHCONHCH(OC2H5)CCIs
I ¦ j
(C6H5NHC0NHCHCC13)20 !
CeH5NHCONHCH(OCH3)CB|r3
CeH5NHCONHCH(OC2H5)CEr3
і ;
(C6H5NHCONHCHCBr3)20 і «-ClCeH4NHCONHCH(OC4If9-H)CH3 jM-02NCeH4NHCONHCH(OQH3)CCl3 JM-O2NCeH4NHCONHCH(O(I2H5)CCl3
(JM-O2NCeH4NHCONHCHCGIs)2O «-O2NC6H4NHCONHCH(OdH3)CCl3
73
161
161
161
161
161, 473 162 162 162
162 161
163
163 163
163 163 163 163 163
163 234 161 161
.161 163 163
163
234 (60)
227
227
227 227
216
Продолжение табл. 25
Простые эфиры N-a-оксиалкильных производных
Литература <выход, %)
/j-O2NCeH4NHGONHCH(OC2H5)CCl3 I
(n-02NC6H4NHCONHCHCCl3)20
0-CH3CeH4NHCONHCH(OCH3)CCl3
0-CH3CeH4NHCONHCH(OC2H5)CCl3
(0-CH3CeH4NHCONHCHCCl3)2O «-CH3CeH4NHCONHCH(OCH3)CCl3 «-CH3CeH4NHCONHCH(OC2H5)CCl3 I
(«-CH3CeH4NHCONHCHCCl3)20
CH3CONHCONHCH(OCh3)CCI3
CH3CONHCONHCH(Oc2H5)CCI3
I
(CH3CONHCONHCHCCl3)20 CO[NHCH(OCh3)CCI3I2 CO[NHCH(OC2H5)CCl3]2 CO[NHCH(OC3H7-k)CC13]2 CO[NHCH(OCH3)CBr3J2 CO[NHCH(OC2H5)CBr3I2 ,NHCH(OCH3)CCl3
со'
CO
4NHCH(OC2H5)CBr3 NHCH(OC2H5)CCl3