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Water → Methyl (2,2-dimethylpent-4-en-1-yl)carbamate

HRID 389181
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HRID 389181 반응식
[CH3:1][C:2]([CH3:8])([CH2:5][CH:6]=[CH2:7])[CH2:3][NH2:4].C(N(C(C)C)CC)(C)C.Cl[C:19]([O:21][CH3:22])=[O:20].O>C(Cl)Cl>[CH3:1][C:2]([CH3:8])([CH2:5][CH:6]=[CH2:7])[CH2:3][NH:4][C:19](=[O:20])[O:21][CH3:22]
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참가 물질

6

반응물 4

HCID 962WaterHCID 6586Methyl chloroformateHCID 81531DiisopropylethylamineHCID 6418312,2-Dimethylpent-4-en-1-amine

생성물 1

HCID 45123004Methyl (2,2-dimethylpent-4-en-1-yl)carbamate

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
0 °C

실험 절차

A 1 L round-bottom flask under nitrogen was charged with 2,2-Dimethylpent-4-en-1-amine (9.86 g, 87 mmol), diisopropylethylamine (16.73 ml, 96 mmol), and DCM (100 mL) and cooled to 0° C. A solution of methyl chloroformate (7.08 mL, 91 mmol) in DCM (50 mL) was added dropwise. The reaction mixture was warmed to RT, stirred for 24 hours and poured into water. The mixture was extracted with EtOAc (3×). The combined organic portions were washed with brine, dried with anhydrous MgSO4 and filtered, and the solvent was removed from the filtrate by rotary evaporation. The crude product was purified by silica gel chromatography eluting with 70 hexane/30 EtOAc, to give the title compound. 1H NMR (CDCl3): δ 5.85-5.79 (m, 1H), 5.06-5.02 (m, 2H), 4.46 (s, 1H), 3.67 (s, 3H), 3.02-3.00 (m, 2H), 1.98-1.96 (m, 2H), 0.88 (s, 6H) ppm.

후처리

  1. temperatureThe reaction mixture was warmed to RT
  2. extractionThe mixture was extracted with EtOAc (3×)
  3. washThe combined organic portions were washed with brine
  4. dry with materialdried with anhydrous MgSO4
  5. filtrationfiltered
  6. customthe solvent was removed from the filtrate by rotary evaporation
  7. customThe crude product was purified by silica gel chromatography
  8. washeluting with 70 hexane/30 EtOAc

출처 및 근거

ORD 기록
ord-9a06fb77b72540698b84e4308fb003e4
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08377874B2

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