Органические реакции, Сборник 14 - Коп А.
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164 , 460 (78)
K-C4H9CONHCHOHCCI2CHCICh3
460 (69)
«3o-C4H9CONHCHOHCC13-
460 (41)
«3OJC4H9CONHCHOHCBr3
207
«30-IC4H9CONHCHOHCCi2CHCICH3
460 (14)
(CH8)2CHCHBrCONHCHOHCCl3 .
468
K-C^H11CONHCHOHCCi3
164 , 460 (69)
197
Продолжение табл. 23
а-Оксиалкиламидопроизводное
Литература (выход, %)
K-C5H11CONHCHOHCBr3
207
K-c5HJ1conhchohcci2chcich3
460 (62)
(C2H5)2CHCONHCHOHCCl3
460 (78)
<C2H5)2CHCONHCHOHCCl2CHClCH3
460 (42)
K-CeH13CONHCHOHCCl3
164, 460 (81)
K-CeH13CONHCHOHCBr3
207
K-c6h13conhchohcci 2СНС1CH3
460 (72)
K-c7h15conhchohcci3
460 (100)
K-C7H15CONHCHOHCBr3
207
K-c7h15conhchohcci jjCHCl CH3
460 (66)
K-c4h9ch(c2h5)conhchohcci3
460 (88)
H-c8h17conhchohcci3
460 (76)
K-c8h17conhchohcci2chcich3
460 (57)
H-c9h19conhchohcci3
460 (59)
K-C9H19CONHCHOHCBr3
207
K-c9h19conhchohcci2chcich3
460 (43)
H-c15h31conhchohcci3
469
CH2 = chconhchohcci3
її—Ti
101 (66)
Ij4 jch = chconhchohcci3
о
oc-nchohcci3
204 (30)
172
I I
Cl3CCH CHCCl3
о
Из ароматических амидов
c6h5conhchohchci2 а)
208
C6H5CONHCHOHCHBr2 а)
208
c6h5conhchohcci3
95, 171, 158, 47
C6H5CONHCHOHCBrCl2 а)
208
C6H5CONHCHOHCBr3
166, 208
c6h5conhchohcci2chcich3
463, 464
0-hoc6h4conhchohcci3
364
0-HOC6H4CONHCHOHCBr3
166
Af-HOC6H4CONHCHOHCC]3
170 (0)
n-HOC6H4CONHCHOHCCl3
171 (0)
2-HO-3-ClC6H3CONHCHOHCCl3
171 (81), 470а
2-HO-5-ClC6H3CONHCHOHCCl3
171 (65)
198
199
Продолжение табл. 23
а-Оксиалкиламидопроизводное
Литература (выход, %)
2-HO-3,5-Cl2C6H2CONHCHOHCCl3
2-HO-3-BrC6H3CONHCHOHCCl 3
2-HO-5-BrC6H3CONHCHOHCCl3
2-HO-3,5-Br2C6H2CONHCHOHCCl3
2-HO-3-02NCeH3CONHCHOHCCl3
2-HO-5-Br-3-02NC6H2CONHCHOHCCl3
2-HO-3,5-(02N)2C6H2CONHCHOHCCl3
2-HO-5-CH3CONHC6H3CONHCHOHCCl3
0-CH3OC6H4CONHCHOHCCi3
X-CH3OC6H4CONHCHOHCCi3
n-CH3OC6H4CONHCHOHCCl3
2-CH30-3-ClC6H3CONHCHOHCCl3
2-CH30-5-ClC6H3CONHCHOHCCl3
2-CHgO-3,5-Cl2C6H2CONHCHOHCCl3
2-CH30-2-BrC6H3CONHCHOHCCl3
2-CH30-3,5-Br2C6H2CONHCHOHCCl3
2-CH30-3-02NC6H3CONHCHOHCCl3
2-CH30-5-02NC6H3CONHCHOHCCl3
2-CH30-3,5-(02N)2C6H2CONHCHOHCCl3
0-CH3CO2C6H4CONHCHOHCCi3
e-CH3CONHC6H4CONHCHOHCCl3
X-CH3CONHC6H4CONHCHOHCCi3
n-CH3CONHC6H4CONHCHOHCCl3
2-CH3CONH-5-BrC6H3CONHCHOHCCl3
0-C6H5CONHC6H4CONHCHOHCCi3
X-C6H5CONHC6H4CONHCHOHCCi3
n-C6H5CONHC6H4CONHCHOHCCl3 2-C6H5CONH-5-BrC6H3CONHCHOHCC i3 0-CH3C6H4CONHCHOHCCi3 X-CH3C6H4CONHCHOHCCi3 H-CH3C6H4CONHCHOHCCi3
^ \ ^\ — CONHCHOHCCi3
Cl3C O x/
Из гетероароматических амидов
O- CONHCHOHCCi3
о
171 (82) 169 169 169
169 (77) 169 (96)
169 (85) 372 (68)
166, 171 (хороший)
171 (хороший)
171 (хороший)
171 (82)
171 (79)
171 (79)
169
169
169
169
169
364
170 (90) 170 (85) 170 (90) 170 (85) 170
170 (90) 170 (60) 170 (75) 168 168
166, 168 165
204 (86)
Продолжение табл. 23
а-Оксиалкиламидопроизводиое
Литература (выход, %)
Д J-CONHCHOHCCi3 Br' 0
204 (84)
/| l—CONHCHOHCCU
п—п
204 (64)
Д JJ- CONHCHOHCCi3
204 (74)
/| 1-CONHCHOHCCi3 (CH3I3CZV
204 (91)
j^CONHCHOHCClg
471
•ч /
N
Из дикарбоксамидов
(CONHCHOHCCl3)2
163 (31)
C6H5NHCOCONHCHOHCCi3
163
CH2(CONHCHOHCCIg)2
166
C2H5CH(CONHCHOHCCl3)2
163
(C2Hj)2C(CONH2)CONHCHOHCCIg
286
C6H5NHCOCH(C2H5)CONHCHOHCCIg
163
CCl3CHOHCH(CONHCHOHCCl3)2
163
C6H5NHCOCH(CHOHCCi3)CONHCHOH
163
CCl3
(CH2CONHCHOHCCl3)2
166
Из лактамов
NH
со чснон
I I
C6H5C CH2
174
I CH2
CH2CH2N(C2Hs)2
200
Продолжение табл. 23
а-Оксиалкиламидрпроизводиое
Литература (выход, %)
nh
со хснон CeH5C—Ch2
N.
\-
^\-снон 4nh
\/~С0
^4—choh 4nch3
\/-С0
^4,—choh
\
nc6h5
-со
^4—choh
\
х/~
^V-choh
\
^nc6h4no2-Zi со
nc6h4och3-O —со
—choh
4nc6h4och3-k со
^4,—choh
\
/
—со
nc6h4ch3-O
174 (30)
175 (66)
175^(66)
175 (23)
175 (81)
175^(27)
175(18)
175 (23)
201
Продолжение табл. 23
а-Оксвалкиламидопроизводиое
' Литература (выход, %)
^4,—CHOH
NC6H4CH3-k \/'-с°
^4,—CHOH _
-ссГ >=<
\_/
CH
Из карбамильных соединений
CH3O2CNHCHOHCCi3
C2H5O2CNHCHOHCCi3
C2H5O2CNHCHOHCBr3
C2H5O2CNHCHOHCCI2CHCICh3
C2H5O2CNHC(OH)(CF2Cl)2
«-C3H7O2CNHCHOHCCi3
«30-C4H9O2CNHCHOHCCi3
«30-C5H11O2CNHCHOHCCi3
MeHTIW-O2CNHCHOHCCl3
BOPHIM-O2CNHCHOHCCi3
H2NCONHCHOHCCi3
CO(NHCHOHCCl3)2
175 (40)
175 (37)
472
472
95(100), 167
94 (100), 95, 167, 173, 229
173
173
73
167 (96)
167
95
95
160
158, 161, 73, 158, 473 (71)
162, 473 (66) 160, 161, 162,
202
Продолжение табл. 23
а-Оксиалкнламндопроизводное
Литература (выход, %)
yNHCHOHCCl3
со
162, 474
4^NHCHOHCBr3
^NHCHOHCCi3
со
161
4NHCH(OCH3)CCl3
