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

Chlorotrimethylsilane → 2,5-Pyrrolidinedione, 1-(trimethylsilyl)-

HRID 893900
노트
인쇄 미리보기

반응식

HRID 893900 반응식
[C:1]1(=[O:7])[NH:5][C:4](=[O:6])[CH2:3][CH2:2]1.C(N(CC)CC)C.[CH3:15][Si:16]([CH3:19])([CH3:18])Cl>C1(C)C=CC=CC=1>[CH3:15][Si:16]([CH3:19])([CH3:18])[N:5]1[C:4](=[O:6])[CH2:3][CH2:2][C:1]1=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6397ChlorotrimethylsilaneHCID 8471TriethylamineHCID 11439Succinimide

생성물 1

HCID 116654792,5-Pyrrolidinedione, 1-(trimethylsilyl)-

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To 400 g (4 moles) of succinimide and 900 ml of triethylamine in 2700 ml of toluene 780 ml of trimethylchlorosilane were added in two hours with vigorous stirring. After refluxing and stirring for an additional hour the mixture was allowed to cool to room temperature. The precipitate was filtered off, washed with 1 l of toluene and 1 l of light petrol (40°-60° C.) and the combined filtrate and washings concentrated to about 700 ml. N-trimethylsilylsuccinimide was isolated by distillation at diminished pressure. The yield was 573 g (3.35 moles) or 83.5%; boiling point 62° C./0.3 mm Hg.

후처리

  1. temperatureAfter refluxing
  2. filtrationThe precipitate was filtered off
  3. washwashed with 1 l of toluene and 1 l of light petrol (40°-60° C.)
  4. concentrationthe combined filtrate and washings concentrated to about 700 ml

출처 및 근거

ORD 기록
ord-8668dde6452545ec8d766381655a7a35
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04282145

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트