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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Neopentyl alcohol → HCID 545965, 화합물

HRID 1380114
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HRID 1380114 반응식
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7](Cl)=[O:8].[CH3:10][C:11]([CH3:15])([CH3:14])[CH2:12][OH:13]>C1C=CC=CC=1>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:13][CH2:12][C:11]([CH3:15])([CH3:14])[CH3:10])=[O:8]
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참가 물질

4

반응물 2

HCID 6404Neopentyl alcoholHCID 898486-Bromohexanoyl chloride

생성물 1

HCID 545965HCID 545965, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A solution of 6-bromohexanoyl chloride (10.0 g, 0.047 mol) and 2,2-dimethylpropanol (4.96 g, 0.056 mol) in benzene (100 ml) was heated under reflux for 2 hours. The solvent was evaporated off under reduced pressure and the residue was dissolved in dichloromethane (200 ml), washed with aqueous sodium hydroxide (2M, 50 ml), water (50 ml) and dried (Na2SO4). The solvent was evaporated off under reduced pressure to give the crude product which was further purified by column chromatography (alumina, dichloromethane) to give neopentyl 6-bromohexanoate as a colourless oil.

후처리

  1. temperatureunder reflux for 2 hours
  2. customThe solvent was evaporated off under reduced pressure
  3. dissolutionthe residue was dissolved in dichloromethane (200 ml)
  4. washwashed with aqueous sodium hydroxide (2M, 50 ml), water (50 ml)
  5. dry with materialdried (Na2SO4)
  6. customThe solvent was evaporated off under reduced pressure
  7. customto give the crude product which
  8. customwas further purified by column chromatography (alumina, dichloromethane)

출처 및 근거

ORD 기록
ord-3156752c4bdd44f989541f8618d566ec
출처 데이터셋
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04579862

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