Acetic Anhydride → Ethyl 6-acetoxymethylnicotinate

HRID 1030511노트

반응식

HRID 1030511 반응식
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[CH:8][C:9]([CH3:13])=[N+:10]([O-])[CH:11]=1)=[O:5])[CH3:2].[C:14]([O:17]C(=O)C)(=[O:16])[CH3:15]>>[C:14]([O:17][CH2:13][C:9]1[CH:8]=[CH:7][C:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])=[CH:11][N:10]=1)(=[O:16])[CH3:15]

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 15045502Ethyl 6-methyl-1-oxo-1lambda~5~-pyridine-3-carboxylate

생성물 1

HCID 15045503Ethyl 6-acetoxymethylnicotinate수율 59.2%

실험 절차

A mixture of 13.7 g of 5-ethoxycarbonyl-2-methyl-pyridine-1-oxide and 15 g of acetic anhydride was stirred under reflux. Excess acetic anhydride was removed under a reduced pressure, and the residue was purified by distillation under a reduced pressure (110° C./0.1 mmHg) to obtain 10.0 g of ethyl 6-acetoxymethylnicotinate. ##STR7##

후처리

  1. temperatureunder reflux
  2. customExcess acetic anhydride was removed under a reduced pressure
  3. distillationthe residue was purified by distillation under a reduced pressure (110° C./0.1 mmHg)

출처 및 근거

ORD 기록
ord-f82664c3b79d43438b9e0c0700f733fd
출처 데이터셋
uspto-grants-1992_04
특허 번호
US05106859

반응 노트

불러오는 중…