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Pyridine → Chloromethyl 3-methylbutyl carbonate

HRID 2295779
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반응식

HRID 2295779 반응식
[CH3:1][CH:2]([CH3:6])[CH2:3][CH2:4][OH:5].N1C=CC=CC=1.Cl[C:14]([O:16][CH2:17][Cl:18])=[O:15]>ClCCl>[C:14](=[O:15])([O:5][CH2:4][CH2:3][CH:2]([CH3:6])[CH3:1])[O:16][CH2:17][Cl:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 31260Isoamyl AlcoholHCID 62754Chloromethyl chloroformate

생성물 1

HCID 13269181Chloromethyl 3-methylbutyl carbonate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3-Methyl-1-butanol (4.4 g) was dissolved in dichloromethane (75 ml) and pyridine (4.0 g) was added to it. The reaction mixture was cooled in an ice bath and chloromethyl chloroformate (6.5 g) was added to it with stirring. The cooling bath was removed and the reaction mixture was stirred at room temperature for 16 hours. The dichloromethane solution was washed with water thrice and once with brine. The organic layer was dried over sodium sulfate and evaporated to furnish a colorless oil of desired product weighing 10.7 g which was the pure chloromethyl isopentyl carbonate. NMR (CDCl3) δ 0.95 (6H, d, J=5 Hz, CH(CH3)2), 1.66 (3H, m, CH2 and CH), 4.28 (2H, t, J=7 Hz, OCH2CH2) and 5.73 (2H, s, OCH2Cl). IR (film) 2950, 1783, 1265 cm-1.

후처리

  1. temperatureThe reaction mixture was cooled in an ice bath
  2. customThe cooling bath was removed
  3. stirringthe reaction mixture was stirred at room temperature for 16 hours
  4. washThe dichloromethane solution was washed with water thrice and once with brine
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. customevaporated

출처 및 근거

ORD 기록
ord-6ede1b901447430681bc22c35136c058
출처 데이터셋
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04426391

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