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Hydrochloric Acid → 7-Chloro-2-(5-hydroxymethylbenzofuran-2-yl)quinoline

HRID 2258514
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인쇄 미리보기

반응식

HRID 2258514 반응식
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:12]3[O:13][C:14]4[CH:20]=[CH:19][C:18]([CH:21]=[O:22])=[CH:17][C:15]=4[CH:16]=3)=[N:9]2)=[CH:4][CH:3]=1.[BH4-].[Na+].Cl.C(=O)([O-])O.[Na+]>CO.C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:12]3[O:13][C:14]4[CH:20]=[CH:19][C:18]([CH2:21][OH:22])=[CH:17][C:15]=4[CH:16]=3)=[N:9]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 4311764Sodium borohydrideHCID 229221457-Chloro-2-(5-formylbenzofuran-2-yl)quinoline

생성물 1

HCID 229221977-Chloro-2-(5-hydroxymethylbenzofuran-2-yl)quinoline수율 87.5%

시약·촉매·용매 2

HCID 887
Methanol
용매
HCID 6212Chloroform용매

실험 절차

To a cooled solution of 7-chloro-2-(5-formylbenzofuran-2-yl)quinoline (0.92 g) in a mixture of methanol (20 ml) and chloroform (10 ml) was added sodium borohydride (0.40 g) in small portions. After being stirred at the same temperature for 2 hours, the resulting mixture was treated with diluted hydrochloric acid and adjusted to be basic with aqueous sodium hydrogen carbonate. The resulting precipitates were collected by filtration, Washed with water and dried to give 7-chloro-2-(5-hydroxymethylbenzofuran-2-yl)quinoline (0.81 g).

후처리

  1. customThe resulting precipitates
  2. filtrationwere collected by filtration
  3. washWashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-b55952b059ce49779fe5ab79b2cde8a8
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05661159

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