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Toluene → 4-Ethoxycarbonylmethoxybutyric acid chloride

HRID 487491
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HRID 487491 반응식
[CH2:1]([O:3][C:4]([CH2:6][O:7][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=O)=[O:5])[CH3:2].C1(C)C=CC=CC=1.C(Cl)(=O)C([Cl:24])=O>CN(C)C=O>[CH2:1]([O:3][C:4]([CH2:6][O:7][CH2:8][CH2:9][CH2:10][C:11]([Cl:24])=[O:13])=[O:5])[CH3:2]
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참가 물질

5

반응물 3

HCID 1140TolueneHCID 65578Oxalyl chlorideHCID 223185004-Ethoxycarbonylmethoxybutyric acid

생성물 1

HCID 543801394-Ethoxycarbonylmethoxybutyric acid chloride

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
50 °C

실험 절차

36 g (0.19 mol) of 4-ethoxycarbonylmethoxybutyric acid are charged to 180 ml of toluene and 0.1 ml of dimethyl formamide is added. Then 24.4 ml (0.28 mol) of oxalyl chloride are added dropwise over 30 minutes. When the addition is complete, the reaction mixture is heated to 50° C., stirred for 1 hour and concentrated by evaporation. Distillation of the residue gives 4-ethoxycarbonylmethoxybutyric acid chloride as a clear colourless liquid of b.p. 87°-89° C./2.10-2 torr.

후처리

  1. additionis added
  2. additionWhen the addition
  3. concentrationconcentrated by evaporation
  4. distillationDistillation of the residue

출처 및 근거

ORD 기록
ord-d3a0c92a93c04f968a9d7f48ee15fbac
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05294734

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