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Boron tribromide → 5-Chloro-2-(4-hydroxyphenylamino)benzoic acid

HRID 2413273
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반응식

HRID 2413273 반응식
B(Br)(Br)Br.[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([NH:15][C:16]2[CH:21]=[CH:20][C:19]([O:22]C)=[CH:18][CH:17]=2)=[C:10]([CH:14]=1)[C:11]([OH:13])=[O:12].C(=O)=O.C(Cl)Cl>C(Cl)Cl>[Cl:5][C:6]1[CH:7]=[CH:8][C:9]([NH:15][C:16]2[CH:21]=[CH:20][C:19]([OH:22])=[CH:18][CH:17]=2)=[C:10]([CH:14]=1)[C:11]([OH:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25134Boron tribromideHCID 133714805-Chloro-2-(4-methoxyphenylamino)benzoic acidHCID 21247280dichloromethane Drikold

생성물 1

HCID 204306985-Chloro-2-(4-hydroxyphenylamino)benzoic acid수율 81%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Boron tribromide (250 ml, 0.8 molar) in methylene dichloride was added dropwise over a period of 70 minutes to a mixture of 25.1 g of 5-chloro-2-(4-methoxyphenylamino)benzoic acid and 125 ml of dry methylene dichloride cooled to -70° C. (Dry Ice/methylene dichloride). The cooling bath was removed and the reaction mixture stirred for about 20 hours. The volatile solvent was stripped off and water (400 ml) was added dropwise to the residue cooled in an ice bath. The mixture was then made basic by addition of potassium carbonate and then acidified with dropwise addition of hydrochloric acid. The solid was collected by filtration and dried to give 19.3 g of 5-chloro-2-(4-hydroxyphenylamino)benzoic acid.

후처리

  1. customThe cooling bath was removed
  2. additionwater (400 ml) was added dropwise to the residue
  3. temperaturecooled in an ice bath
  4. additionThe mixture was then made basic by addition of potassium carbonate
  5. additionacidified with dropwise addition of hydrochloric acid
  6. filtrationThe solid was collected by filtration
  7. customdried

출처 및 근거

ORD 기록
ord-24c2183c37be43e7af6d96555ff3b8d3
출처 데이터셋
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04496590

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