Ethyl orthoformate → HCID 54487700, 화합물

HRID 1288747노트

반응식

HRID 1288747 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:15])[CH2:9][C:10]([CH:12]2[CH2:14][CH2:13]2)=[O:11])=[C:4]([S:16]([CH3:19])(=[O:18])=[O:17])[CH:3]=1.[CH:20](OCC)(OCC)[O:21][CH2:22][CH3:23]>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:15])[C:9](=[CH:20][O:21][CH2:22][CH3:23])[C:10]([CH:12]2[CH2:13][CH2:14]2)=[O:11])=[C:4]([S:16]([CH3:19])(=[O:18])=[O:17])[CH:3]=1

참가 물질

4

반응물 2

HCID 31214Ethyl orthoformateHCID 545513651-[4-Chloro-2-(methanesulfonyl)phenyl]-3-cyclopropylpropane-1,3-dione

생성물 1

HCID 54487700HCID 54487700, 화합물수율 99.7%

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

A mixture of 1-(4-chloro-2-methylsulphonylphenyl)-3-cyclopropylpropan-1,3-dione (7.1 g) and triethyl orthoformate (6.9 g) in acetic anhydride was stirred and heated at reflux for 2 hours. The mixture was evaporated to dryness, toluene was added and the solution was re-evaporated to give 1-(4-chloro-2-methylsulphonylphenyl)-3-cyclopropyl-2-ethoxymethylenepropan-1,3-dione (8.4 g) as a red gum which was not purified further.

후처리

  1. temperatureheated
  2. temperatureat reflux for 2 hours
  3. customThe mixture was evaporated to dryness, toluene
  4. additionwas added
  5. customthe solution was re-evaporated

출처 및 근거

ORD 기록
ord-36e70881e8d242ad90110b7261ec6759
출처 데이터셋
uspto-grants-1998_05
특허 번호
US05747424

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