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

HRID 2203

Reaction equation

HRID 2203 reaction equation
[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]

Participants

5

Procedure

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) δ 7.95(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 C12H13ClO4 : C, 56.1; H, 5.0. found: C, 55.8; H, 5.1%.

Workup

  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

Sources & evidence

ORD record
ord-4789241e5b8e4d179a6429cc6ce17888
Source dataset
uspto-grants-1998_03
Patent number
US05728701

Linked notes

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