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Pyridine → Chloromethyl 3-methylbutyl carbonate

HRID 2295779
ノート
印刷プレビュー

反応式

HRID 2295779 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1049PyridineHCID 31260Isoamyl AlcoholHCID 62754Chloromethyl chloroformate

生成物 1

HCID 13269181Chloromethyl 3-methylbutyl carbonate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-6ede1b901447430681bc22c35136c058
出典データセット
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04426391

反応ノート

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