Acetic Acid → 1,4-Bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene

HRID 444126노트

반응식

HRID 444126 반응식
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=O)[CH3:11])=[CH:6][CH:5]=1)(=O)[CH3:2].[C:13]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])#[N:14].[C:21]([O-:24])(=[O:23])[CH3:22].[NH4+:25].[C:26](O)(=O)[CH3:27].[C:30]1(C)C=CC=CC=1>O>[C:16]([C:15]([C:13]#[N:14])=[C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]([CH3:11])=[C:22]([C:30]#[N:25])[C:21]([O:24][CH2:26][CH3:27])=[O:23])=[CH:6][CH:5]=1)[CH3:2])([O:18][CH2:19][CH3:20])=[O:17]

참가 물질

7

반응물 5

HCID 176Acetic AcidHCID 1140TolueneHCID 7764Ethyl cyanoacetateHCID 138881,4-DiacetylbenzeneHCID 517165Ammonium Acetate

생성물 1

HCID 33932701,4-Bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of p-diacetylbenzene (20.25 g, 0.125 mole), ethyl cyanoacetate (28.3 g, 0.25 mole), ammonium acetate (3.85 g) and acetic acid (10 g) was combined in a 500 ml glass round-bottom flask with toluene (150 ml) and refluxed for 12 hours. A Dean-Stark trap was employed to trap water formed during the reaction. Refluxing was discontinued and the solvent evaporated. The residue containing crude product was distilled under reduced pressure. One fraction, boiling point range 177° C.-195° C. (0.6 mm) amounting to 20.6 g was identified as predominately the 1:1 condensation product. A second fraction, boiling point ~200° C. yielded 18.2 g of 1,4-bis(2-carbethoxy-2-cyano-1-methylethenyl)benzene.

후처리

  1. temperaturerefluxed for 12 hours
  2. customA Dean-Stark trap was employed to trap
  3. temperatureRefluxing
  4. customthe solvent evaporated
  5. additionThe residue containing crude product
  6. distillationwas distilled under reduced pressure
  7. custompoint range 177° C.-195° C. (0.6 mm) amounting
  8. customthe 1:1 condensation product

출처 및 근거

ORD 기록
ord-d764701e8bc64cfb8a45efabc7211bdc
출처 데이터셋
uspto-grants-1981_04
특허 번호
US04263209

반응 노트

불러오는 중…