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Triethylamine → 5-(Chloromethyl)-3-(propan-2-yl)-1,2-oxazole

HRID 2071069
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HRID 2071069 반응식
[CH:1](=[N:5][OH:6])[CH:2]([CH3:4])[CH3:3].[CH2:7]([Cl:10])[C:8]#[CH:9].CCN(CC)CC.Cl([O-])=O.[Na+]>C(Cl)Cl>[Cl:10][CH2:7][C:8]1[O:6][N:5]=[C:1]([CH:2]([CH3:4])[CH3:3])[CH:9]=1
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 9023Propanal, 2-methyl-, oximeHCID 122213-Chloro-1-propyneHCID 23668197Sodium Chlorite

생성물 1

HCID 123646025-(Chloromethyl)-3-(propan-2-yl)-1,2-oxazole수율 62.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirring solution of 1.0 g (11.5 mmol) of isobutyraldehyde oxime, 0.9 g (12.1 mmol) of propargyl chloride, and 0.7 mL (5.02 mmol) of Et3N in 30 mL of CH2Cl2 at 0° C. was added 125 mL of sodium chlorite solution (>4% chlorine). The ice bath was removed and stirring was continued with warming to r.t. After 1.5 h, CH2Cl2 was added, and the organic layer was washed with 20 mL of brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (10% EtOAc/hexanes) provided 1.14 g of 5-(chloromethyl)-3-isopropylisoxazole as a pale yellow liquid in about 62% yield. (60%)

후처리

  1. customThe ice bath was removed
  2. additionCH2Cl2 was added
  3. washthe organic layer was washed with 20 mL of brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customPurification by flash silica gel chromatography (10% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-56c5ea9e0d2c458998609f1b22e10d32
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299267B2

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