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1,3-Difluoroacetone → HCID 86706177, 화합물

HRID 2176328
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HRID 2176328 반응식
[CH2:1]([O:3][C:4](=[O:12])[C:5]([CH2:10][OH:11])([CH2:8][OH:9])[CH:6]=[CH2:7])[CH3:2].[F:13][CH2:14][C:15]([CH2:17][F:18])=O>>[CH2:1]([O:3][C:4]([C:5]1([CH:6]=[CH2:7])[CH2:8][O:9][C:15]([CH2:17][F:18])([CH2:14][F:13])[O:11][CH2:10]1)=[O:12])[CH3:2]
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참가 물질

3

반응물 2

HCID 2283971,3-DifluoroacetoneHCID 86706156HCID 86706156, 화합물

생성물 1

HCID 86706177HCID 86706177, 화합물수율 77.5%

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온도
100 °C

실험 절차

A vial was loaded with 2,2-bis-hydroxymethyl-but-3-enoic acid ethyl ester (0.88 g, 5.05 mmol), 1,3-difluoroacetone (0.95 g, 10.1 mmol) and para-toluene-4-sulfonic acid monohydrate (0.96 g, 5.05 mmol). The vial was sealed and heated in a microwave reactor at 100° C. for 15 min. The resultant brown oil was partitioned between dichloromethane and aqueous sodium bicarbonate solution. The organic layer was filtered through a hydrophobic frit and evaporated to give a brown oil (0.98 g). The oil was purified by silica gel chromatography using iso-hexanes/ethyl acetate 3:1 to yield the title compound (0.619 g, 74%) as a colorless oil. 1H NMR (300 MHz, CDCl3): δ 1.31 (t, J=7.1 Hz, 3H), 3.96 (d, J=12.0 Hz, 2H), 4.27 (q, J=7.1 Hz, 2H), 4.34-4.69 (m, 6H), 5.22-5.35 (m, 2H), 5.67-5.79 (m, 1H).

후처리

  1. customThe vial was sealed
  2. customThe resultant brown oil was partitioned between dichloromethane and aqueous sodium bicarbonate solution
  3. filtrationThe organic layer was filtered through a hydrophobic frit
  4. customevaporated

출처 및 근거

ORD 기록
ord-b1ac152e9b3345f88746f69ca1d69176
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062092B2

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