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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Benzyl chloroformate → HCID 68928025, 화합물

HRID 595334
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HRID 595334 반응식
[C:1](Cl)(=[O:10])[O:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl.[CH2:13]([NH2:17])/[CH:14]=[CH:15]/[CH3:16].CCN(C(C)C)C(C)C>C(#N)C.[Cl-].[Na+].O>[CH2:13]([NH:17][C:1](=[O:10])[O:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)/[CH:14]=[CH:15]/[CH3:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 10387Benzyl chloroformateHCID 81531DiisopropylethylamineHCID 12602976(2E)-but-2-en-1-amine hydrochloride

생성물 1

HCID 68928025HCID 68928025, 화합물

시약·촉매·용매 2

HCID 6342Acetonitrile용매HCID 57417360Sodium chloride; water용매

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온도
0 °C

실험 절차

Benzyl carbonochloridate (22.8 mL, 167 mmol) was added to a solution of (2E)-but-2-en-1-amine hydrochloride (12.0 g, 112 mmol) and Hunig's base (43.2 g, 330 mmol) in acetonitrile (120 mL) under a nitrogen atmosphere at 0° C. The reaction mixture was stirred under nitrogen at 0° C. for 1 hour and then allowed to warm to ambient temperature. After 3 hours, the reaction mixture was diluted with brine (50 mL) and was extracted with ethyl acetate (3×50 mL). The organic layers were combined, dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford the crude product residue. The crude product residue was purified by silica gel chromatography (ethyl acetate/petroleum ether) to give benzyl (2E)-but-2-en-1-ylcarbamate. MS ESI calc'd. for C12H16NO2 [M+H]+ 206. found 206.

후처리

  1. temperatureto warm to ambient temperature
  2. waitAfter 3 hours
  3. extractionwas extracted with ethyl acetate (3×50 mL)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customto afford the crude product residue
  8. customThe crude product residue was purified by silica gel chromatography (ethyl acetate/petroleum ether)

출처 및 근거

ORD 기록
ord-0d6811525e354b4bbd18624e03175c36
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242984B2

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