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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl chloroformate → Methyl hept-6-en-2-ynoate

HRID 1664252
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HRID 1664252 반응식
[CH2:1]([Mg]Br)[CH:2]=[CH2:3].[CH2:6](Cl)[C:7]#[CH:8].Cl[C:11]([O:13][CH3:14])=[O:12]>CCOCC>[C:11]([O:13][CH3:14])(=[O:12])[C:3]#[C:2][CH2:1][CH2:8][CH:7]=[CH2:6]
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참가 물질

5

반응물 3

HCID 6586Methyl chloroformateHCID 122213-Chloro-1-propyneHCID 178455850HCID 178455850, 화합물

생성물 1

HCID 59644062Methyl hept-6-en-2-ynoate수율 44%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A solution of allylmagnesium bromide (1M, 150 mL, 150 mmol) in ether under a nitrogen atmosphere was cooled to −10° C., and propargyl chloride (5.4 mL, 75 mmol) was added dropwise. The solution was stirred for 24 h at room temperature, and then cooled to 0° C. Methyl chloroformate was added dropwise, and the solution was allowed to stir at room temperature for 4 h. The reaction was quenched by cautious addition of satd aq NH4Cl (100 mL) at 0° C. The organic layer was washed with brine, dried, and evaporated to a residue. Chromatography on silica gel provided the title compound (4.5 g, 44%) as a pale yellow liquid.

후처리

  1. temperaturecooled to 0° C
  2. stirringto stir at room temperature for 4 h
  3. customThe reaction was quenched by cautious addition of satd aq NH4Cl (100 mL) at 0° C
  4. washThe organic layer was washed with brine
  5. customdried
  6. customevaporated to a residue

출처 및 근거

ORD 기록
ord-71784f9d46fc4fe59851ac6dc36d3d40
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08039465B2

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