홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium borohydride → HCID 53999561, 화합물

HRID 1164079
노트
인쇄 미리보기

반응식

HRID 1164079 반응식
[BH4-].[Na+].[CH3:3][O:4][C:5]1[C:12]([S:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[Cl:20])=[CH:11][CH:10]=[CH:9][C:6]=1[CH:7]=[O:8]>CO>[CH3:3][O:4][C:5]1[C:12]([S:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[Cl:20])=[CH:11][CH:10]=[CH:9][C:6]=1[CH2:7][OH:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 205134222-Methoxy-3-(2-chlorophenylthio)benzaldehyde

생성물 1

HCID 53999561HCID 53999561, 화합물수율 98.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Sodium borohydride (550 mg) was added in 10 minutes to a solution of 2-methoxy-3-(2-chlorophenylthio)benzaldehyde (9.1 g) in methanol (50 ml) with stirring at temperature below 15° C. After stirring the mixture at room temperature for 30 minutes, methanol was distilled off under reduced pressure. The residue was dissolved in water, acidified with conc. hydrochloric acid and extracted with diethyl ether. The extract was washed with water, dried and then evaporated under reduced pressure to give oily 2-methoxy-3-(2-chlorophenylthio)benzyl alcohol (9 g).

후처리

  1. stirringAfter stirring the mixture at room temperature for 30 minutes
  2. distillationmethanol was distilled off under reduced pressure
  3. dissolutionThe residue was dissolved in water
  4. extractionextracted with diethyl ether
  5. washThe extract was washed with water
  6. customdried
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-4d451cb6606349dd99d0f09b16384c7b
출처 데이터셋
uspto-grants-1983_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04367238

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트