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

Sodium Hydroxide → 1-(4-Ethynylbenzyl)pyrrolidine

HRID 735005
노트
인쇄 미리보기

반응식

HRID 735005 반응식
C[Si]([C:5]#[C:6][C:7]1[CH:18]=[CH:17][C:10]([CH2:11][N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[CH:9][CH:8]=1)(C)C.[OH-].[Na+]>ClCCl.CO>[C:6]([C:7]1[CH:18]=[CH:17][C:10]([CH2:11][N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[CH:9][CH:8]=1)#[CH:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 688167401-(4-Trimethylsilanylethynylbenzyl)pyrrolidine

생성물 1

HCID 860607941-(4-Ethynylbenzyl)pyrrolidine

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

A solution of 0.75 g (2.91 mmol) of 1-(4-trimethylsilanylethynylbenzyl)pyrrolidine in 10 mL of dichloromethane and 10 mL of methanol is combined with 2.4 mL of a 1M sodium hydroxide solution and stirred for 3 hours at ambient temperature. The reaction mixture is evaporated down and the residue is extracted with water and ethyl acetate. The organic phase is stirred with activated charcoal, filtered, and then dried over sodium sulfate. Yield: 0.4 g (74.1% of theory); C13H15N (M=185.27); calc.: molecular ion peak (M+H)+: 186; found: molecular ion peak (M+H)+: 186.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThe reaction mixture is evaporated down
  2. extractionthe residue is extracted with water and ethyl acetate
  3. stirringThe organic phase is stirred with activated charcoal
  4. filtrationfiltered
  5. dry with materialdried over sodium sulfate

출처 및 근거

ORD 기록
ord-b2a57090acf04314b39821dd3ebcb8ff
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07592373B2

반응 노트

불러오는 중…