Hydrochloric Acid → 1-Chloro-3-phenoxypropan-2-one

HRID 2199029Notes

Reaction equation

HRID 2199029 reaction equation
[N+](=[CH2:3])=[N-].[O:4]([CH2:11][C:12](Cl)=[O:13])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[ClH:15]>C(OCC)C>[Cl:15][CH2:3][C:12]([CH2:11][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:13]

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 9550DiazomethaneHCID 69703Phenoxyacetyl chloride

Product 1

HCID 116224561-Chloro-3-phenoxypropan-2-one

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent2×

Procedure

To a stirred solution of diazomethane (ca 6 g=0.141 mmol) in ethyl ether (400 ml) was added over 2 hours at 1°-3° phenoxyacetyl chloride (11.95 g=0.07 mole) dissolved in ethyl ether (50 ml). The mixture was stirred at the same temperature for two more hours and was allowed to stand overnight at room temperature. Then 5.5 N hydrochloric acid (25 ml, 0.137 moles) was added with stirring over 110 min. at 16°-20°. After the mixture was stirred for an additional 4 hours, the layers were separated and the ether layer was washed with three 80 ml portions of water and dried over anhydrous sodium sulfate. Removal of the solvent gave the crude product as a yellow oil, 13 g (100%); ir (film, cm-1) 1740, 1595, 1495, 1240; nmr (DCCl3, ppm) 7.40-6.70 (m, 5H), 4.60 (s, 2H), 4.25 (s, 2H). This product was used without purification to prepare phenoxyacetylmethyltriphenylphosphonium chloride.

Workup

  1. stirringwith stirring over 110 min. at 16°-20°
  2. stirringAfter the mixture was stirred for an additional 4 hours
  3. customthe layers were separated
  4. washthe ether layer was washed with three 80 ml portions of water
  5. dry with materialdried over anhydrous sodium sulfate
  6. customRemoval of the solvent

Sources & evidence

ORD record
ord-c0bfd1843ed842dd9973ab1692123e6b
Source dataset
uspto-grants-1982_11
Patent number
US04361514

Reaction notes

Loading…