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

Ammonium Chloride → 2,3-dihydro-2-(hydroxymethyl)-1H-pyrrolo[1,2-a]indole

HRID 863683
노트
인쇄 미리보기

반응식

HRID 863683 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:7]1[C:11]2=[CH:12][C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:18]=3[N:10]2[CH2:9][CH:8]1[C:19](OCC)=[O:20].[Cl-].[NH4+]>O1CCCC1>[OH:20][CH2:19][CH:8]1[CH2:9][N:10]2[C:18]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[CH:12]=[C:11]2[CH2:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 19696125HCID 19696125, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 196963632,3-dihydro-2-(hydroxymethyl)-1H-pyrrolo[1,2-a]indole수율 58%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

4 ml of a 1M solution of lithium aluminum hydride in tetrahydrofuran were added to a solution of 750 mg of ethyl 2,3-dihydro-1H-pyrrolo[1,2-a]indole-2-carboxylate in 30 ml of tetrahydrofuran. After 1 hour, 30 ml of saturated ammonium chloride solution were added and the mixture was evaporated. The residue was extracted with dichloromethane and the organic extract was dried and evaporated. Crystallization of the residue from diethyl ether/petroleum ether gave 355 mg of 2,3-dihydro-2-(hydroxymethyl)-1H-pyrrolo[1,2-a]indole of melting point 76°-78° C.

후처리

  1. customthe mixture was evaporated
  2. extractionThe residue was extracted with dichloromethane
  3. extractionthe organic extract
  4. customwas dried
  5. customevaporated
  6. customCrystallization of the residue from diethyl ether/petroleum ether

출처 및 근거

ORD 기록
ord-1b4a2dc1665745f19420c6cad0c925f0
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05721245

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트