Sodium Hydroxide → HCID 23669529, compound

HRID 1658012Notes

Reaction equation

HRID 1658012 reaction equation
[CH3:1][O:2][CH2:3][O:4][CH2:5][C:6]([O:8]C)=[O:7].[OH-].[Na+:11]>CO>[CH3:1][O:2][CH2:3][O:4][CH2:5][C:6]([O-:8])=[O:7].[Na+:11]

Participants

4

Procedure

Methyl methoxymethyloxyacetate (19.06 g) in methanol (20 ml.) is treated with aqueous sodium hydroxide (57 ml. of a 2.5 N solution) over a period of 30 minutes. The methanol is evaporated under reduced pressure and the aqueous residue lyophilized giving sodium methoxymethyloxyacetate. The sodium salt is dispersed in benzene (250 ml.) and treated with pyridine (1 ml.). Oxalyl chloride (30 ml.) is added with ice-bath cooling. The resulting mixture is stirred in the cold until gas evolution ceases, then at room temperature for 5 minutes. The mixture is filtered and evaporated under reduced pressure to remove excess oxalyl chloride and benzene. Distillation of the residue gives methoxymethyloxyacetyl chloride.

Workup

  1. customThe methanol is evaporated under reduced pressure

Sources & evidence

ORD record
ord-864522ccc99b4de9bbaa5561eb8ad2ad
Source dataset
uspto-grants-1976_06
Patent number
US03962224

Reaction notes

Loading…