Vinylidene chloride → Ethyl 5-chloro-1,2-oxazole-3-carboxylate

HRID 1057756

反応式

HRID 1057756 の反応式
[CH3:1][CH2:2][O:3][C:4](/[C:6](/Cl)=[N:7]\[OH:8])=[O:5].CCN(CC)CC.[Cl:17][C:18](Cl)=[CH2:19]>>[CH2:2]([O:3][C:4]([C:6]1[CH:19]=[C:18]([Cl:17])[O:8][N:7]=1)=[O:5])[CH3:1]

参加物

4

実験手順

To a solution of ethyl chlorooximidoacetate (11.0 g, 72.6 mmol, 1 equiv) in 1,1-dichloroethylene (350 mL) was added Et3N (25.3 mL, 181 mmol, 2.5 equiv) in 1,1-dichloroethylene (100 mL) via addition funnel over 30 min. The reaction mixture was stirred at room temperature for 23 h, then was partitioned between water (150 mL) and CH2Cl2 (2×150 mL). The combined organic layers were dried over Na2SO4 and were concentrated. The residue was purified by flash column chromatography (10% EtOAc in hexanes) to give the title intermediate (4.49 g, 35%) as a pale yellow oil: IR (cm−1) 1735, 1436, 1253; 1H NMR (CDCl3) δ 1.45 (t, 3H, J=7.2), 4.49 (q, 2H, J=7.2), 7.29 (s, 1H).

後処理

  1. additionvia addition funnel over 30 min
  2. customwas partitioned between water (150 mL) and CH2Cl2 (2×150 mL)
  3. dry with materialThe combined organic layers were dried over Na2SO4
  4. concentrationwere concentrated
  5. customThe residue was purified by flash column chromatography (10% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-eee196f7069440a39edd9f046a80d4cb
出典データセット
uspto-grants-2003_02
特許番号
US06514997B2

関連ノート

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