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N,N-Dimethylaniline → Butanoic acid, 4-chloro-, 1,1-dimethylethyl ester

HRID 130596
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HRID 130596 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][C:5](Cl)=[O:6].CN(C)C1C=CC=CC=1.[C:17]([OH:21])([CH3:20])([CH3:19])[CH3:18]>C(OCC)C>[Cl:1][CH2:2][CH2:3][CH2:4][C:5]([O:21][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:6]
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참가 물질

5

반응물 3

HCID 949N,N-DimethylanilineHCID 6386tert-ButanolHCID 783704-Chlorobutyryl chloride

생성물 1

HCID 527695Butanoic acid, 4-chloro-, 1,1-dimethylethyl ester

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A mixture of 4-chlorobutyryl chloride (93 g, 0.66 mol), N,N-dimethylaniline (80 g, 0.66 mol) and tert-butanol (0.66 mol) in ethyl ether (100 mL) was refluxed for 5 h. The reaction was cooled, diluted with ether and washed with water, 10% citric acid, saturated NaCl and dried over Na2SO4. Crude product obtained after evaporation of the solvent was distilled under vacuum (10 mmHg). Pure product (79 g, 67%) boiling at 57-58° C. was collected. 1H NMR (DMSO-d6) δ 3.64 (t, J=7 Hz, 2H), 2.35 (t, J=7 Hz, 2H), 1.93 (q, 2H), 1.41 (s, 9H).

후처리

  1. temperaturewas refluxed for 5 h
  2. temperatureThe reaction was cooled
  3. washwashed with water, 10% citric acid, saturated NaCl
  4. dry with materialdried over Na2SO4
  5. customCrude product obtained
  6. customafter evaporation of the solvent
  7. distillationwas distilled under vacuum (10 mmHg)
  8. customPure product (79 g, 67%) boiling at 57-58° C. was collected

출처 및 근거

ORD 기록
ord-1faaece79fc84df0b19a0daa1dfc88fb
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07381818B2

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