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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Propionyl chloride → HCID 19838438, 화합물

HRID 476765
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반응식

HRID 476765 반응식
[C:1](Cl)(=[O:4])[CH2:2][CH3:3].Cl.[NH2:7][CH:8]1[CH2:20][C:19]2[C:11](=[CH:12][C:13]3[CH2:17][CH2:16][O:15][C:14]=3[CH:18]=2)[CH2:10][CH2:9]1>C1C=CC=CC=1.C(N(CC)CC)C.O>[C:1]([NH:7][CH:8]1[CH2:20][C:19]2[C:11](=[CH:12][C:13]3[CH2:17][CH2:16][O:15][C:14]=3[CH:18]=2)[CH2:10][CH2:9]1)(=[O:4])[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 62324Propionyl chlorideHCID 19838440HCID 19838440, 화합물

생성물 1

HCID 19838438HCID 19838438, 화합물

시약·촉매·용매 3

HCID 241Benzene용매2회HCID 962Water용매HCID 8471Triethylamine용매

실험 절차

A solution of propionyl chloride in 50 ml of benzene is added dropwise to a solution of 5 g of the compound of Example 2 in 100 ml of benzene and 4.2 ml of triethylamine. After one and a half hours' refluxing, the cooled mixture is diluted with water, separated off after being left to settle and extracted with benzene, and the organic phase is washed with water, dried over anhydrous sodium sulfate and evaporated under vacuum. The dry residue is recrystallized in acetonitrile.

후처리

  1. temperatureAfter one and a half hours' refluxing
  2. customseparated off
  3. waitafter being left
  4. extractionextracted with benzene
  5. washthe organic phase is washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. customevaporated under vacuum
  8. customThe dry residue is recrystallized in acetonitrile

출처 및 근거

ORD 기록
ord-1cc0214918e74f2b82234fdf45941cdf
출처 데이터셋
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04885373

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