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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → HCID 21279517, 화합물

HRID 2291211
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인쇄 미리보기

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HRID 2291211 반응식
[CH2:1]([S:8][C:9]1[N:13]=[C:12]([SH:14])[NH:11][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[CH2:16][C:17](=O)[CH3:18].CCOCC.C(=O)(O)[O-].[Na+]>C(O)C>[CH2:1]([S:8][C:9]1[N:13]=[C:12]2[S:14][CH:16]=[C:17]([CH3:18])[N:11]2[N:10]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 6571ChloroacetoneHCID 516892Sodium BicarbonateHCID 178527897HCID 178527897, 화합물

생성물 1

HCID 21279517HCID 21279517, 화합물수율 92.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The product of stage (a) (22.3 g) and chloroacetone (9.6 g) were heated in ethanol (120 ml) under reflux for 22 hours. The solution was then reduced under vacuum, and the residue was stirred with a mixture of ether and aqueous sodium bicarbonate. The ether solution was separated, washed with water, dried over magnesium sulphate, and reduced under vacuum to give 24.1 g of the desired product as an orange oil.

후처리

  1. temperatureunder reflux for 22 hours
  2. customThe ether solution was separated
  3. washwashed with water
  4. dry with materialdried over magnesium sulphate

출처 및 근거

ORD 기록
ord-69c3e20a77984705bb93987ed50712d5
출처 데이터셋
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04795483

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