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Bromine → HCID 23314490, 화합물

HRID 745137
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HRID 745137 반응식
[C:1]([C:4]1[C:5]([O:15][CH3:16])=[CH:6][C:7]([O:13][CH3:14])=[C:8]([CH:12]=1)[C:9]([OH:11])=[O:10])(=[O:3])[CH3:2].[Br:17]Br>O1CCOCC1>[Br:17][CH2:2][C:1]([C:4]1[C:5]([O:15][CH3:16])=[CH:6][C:7]([O:13][CH3:14])=[C:8]([CH:12]=1)[C:9]([OH:11])=[O:10])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408Bromine2회HCID 3298125-Acetyl-2,4-dimethoxybenzoic acid

생성물 1

HCID 23314490HCID 23314490, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

5-Acetyl-2,4-dimethoxybenzoic acid (Ber. 41, 1607, 1908) (21.1 g, 0.094 mole) was stirred in dioxane (200 ml.) at room temperature and bromine (5 ml., ca 0.1 mole) was added dropwise. The bromine colour gradually disappeared over 30 minutes and the mixture was then gently warmed in a steambath for 30 minutes, cooled and the dioxane removed in vacuo. The solid product was treated with boiling ethyl acetate, filtered hot and the filtrate evaporated to give 5-bromoacetyl-2,4-dimethoxybenzoic acid, m.p. 236° C.

후처리

  1. temperaturethe mixture was then gently warmed in a steambath for 30 minutes
  2. temperaturecooled
  3. customthe dioxane removed in vacuo
  4. additionThe solid product was treated with boiling ethyl acetate
  5. filtrationfiltered hot
  6. customthe filtrate evaporated

출처 및 근거

ORD 기록
ord-92366e5aef104c3a90a0a732fa753227
출처 데이터셋
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE032196

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