Methyl phenoxyacetate → Methyl 4-[3-chloropropanoyl]phenoxyacetate

HRID 743809ノート

反応式

HRID 743809 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[O:5]([CH2:12][C:13]([O:15][CH3:16])=[O:14])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[Cl:17][CH2:18][CH2:19][C:20](Cl)=[O:21]>ClCCl>[Cl:17][CH2:18][CH2:19][C:20]([C:9]1[CH:10]=[CH:11][C:6]([O:5][CH2:12][C:13]([O:15][CH3:16])=[O:14])=[CH:7][CH:8]=1)=[O:21]

参加物

5

実験手順

Aluminium chloride (33.35 g) was added portionwise to a stirred cooled (<0° C.) solution of methyl phenoxyacetate (14.46 ml) and 3-chloropropionyl chloride (9.55 ml) in dichloromethane (500 ml). After the addition the ice-bath was removed and the mixture stirred for 1 hour when it was poured into ice-water (500 ml). The organic phase was separated and the aqueous portion extracted two times with dichloromethane. The combined dichloromethane extracts were washed with water, then brine and dried (MgSO4). The residue, after removal of the solvent in vacuo and trituration with ether gave methyl 4-[3-chloropropanoyl]phenoxyacetate, 22.3 g, as a solid: m.p. 89°-90° C.; NMR (d6DMSO) δ7.95(2H,d), 7.05(2H,d), 4.92(2H,s), 3.91(2H,t), 3.71(3H,s) 3.49(2H,t); m/e 257(M+H)+ ; calculated for C12H13C104 : C, 56.1; H, 5.0. found: C, 55.8; H, 5.1%.

後処理

  1. customwas removed
  2. additionwas poured into ice-water (500 ml)
  3. customThe organic phase was separated
  4. extractionthe aqueous portion extracted two times with dichloromethane
  5. washThe combined dichloromethane extracts were washed with water
  6. dry with materialbrine and dried (MgSO4)
  7. customThe residue, after removal of the solvent in vacuo and trituration with ether

出典と根拠

ORDレコード
ord-8f04f79a38b341a7a5ef31ac6e200199
出典データセット
uspto-grants-1996_09
特許番号
US05556977

反応ノート

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