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

Bromoacetyl bromide → Acetamide, 2-bromo-N-methyl-N-2-propynyl-

HRID 267820
노트
인쇄 미리보기

반응식

HRID 267820 반응식
[CH3:1][NH:2][CH2:3][C:4]#[CH:5].[Br:6][CH2:7][C:8](Br)=[O:9].C(=O)(O)[O-].[Na+]>C(Cl)Cl.CCOCC>[CH3:1][N:2]([CH2:3][C:4]#[CH:5])[C:8](=[O:9])[CH2:7][Br:6]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 61147Bromoacetyl bromideHCID 96160N-methylpropyn-2-ylamineHCID 516892Sodium Bicarbonate

생성물 1

HCID 10774018Acetamide, 2-bromo-N-methyl-N-2-propynyl-수율 85%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매2회HCID 6344Dichloromethane용매2회
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

반응 조건

온도
25 °C

실험 절차

A solution of 13.8 g (0.2 mol) of N-methylpropargylamine in 20 ml methylene chloride was added dropwise to a stirred and cooled (below 15°C.) solution of 40.2 g (0.2 mol) bromoacetyl bromide and 16 g (0.2 mol) sodium bicarbonate in 250 ml methylene chloride. The reaction mixture was allowed to warm to about 25°C. and stirred for 2 hours. The reaction mixture was then filtered and evaporated under reduced pressure to give an oily residue. The residue was diluted with 150 ml ether to form a two-phase mixture consisting of an ether phase and a dark oil. The ether phase was separated, dried over magnesium sulfate, and evaporated to give 32.3 g of N-methyl-N-propargyl-α-bromoacetamide.

후처리

  1. stirringstirred for 2 hours
  2. filtrationThe reaction mixture was then filtered
  3. customevaporated under reduced pressure
  4. customto give an oily residue
  5. customto form a two-phase mixture
  6. customThe ether phase was separated
  7. dry with materialdried over magnesium sulfate
  8. customevaporated

출처 및 근거

ORD 기록
ord-4e2ab9a786d7478fbf79ca559a0316c0
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03944607

반응 노트

불러오는 중…