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Oxalyl chloride → HCID 18628711, 화합물

HRID 1060733
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인쇄 미리보기

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HRID 1060733 반응식
[CH:1]1([CH2:7][CH:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:9](O)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(Cl)(=O)C([Cl:20])=O>C(OCC)(=O)C.CN(C=O)C>[Cl:20][C:9]([CH:8]([CH2:7][CH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1)[C:12]([O:14][CH2:15][CH3:16])=[O:13])=[O:10]
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참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 18628853HCID 18628853, 화합물

생성물 1

HCID 18628711HCID 18628711, 화합물

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

A solution comprised of 3-cyclohexyl-2-ethoxycarbonylpropionic acid (8.52 g, 37 mmol) in ethyl acetate (80 mL) was cooled to 0° C. was treated sequentially with 2 drops of DMF and oxalyl chloride (3.93 mL) added dropwise over five minutes. The mixture was allowed to warm slowly and after approximately 2 hours concentrated to provide ethyl 2-chlorocarbonyl-3-cyclohexylpropionate.

후처리

  1. additionadded dropwise over five minutes
  2. temperatureto warm slowly and after approximately 2 hours
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6e70474a5b134023af8ce676ac455290
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06525036B2

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