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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494480Generated: October 30, 2026

Sodium Chloride → Benzhydryl 2-phthalimidooxyacetate

https://huagongshe.com/reaction/1494480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantBromoacetic AcidHCID 6227—
ReactantN-HydroxyphthalimideHCID 10665—
Reactant1,1'-(Diazomethylene)bis(benzene)HCID 61230—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductBenzhydryl 2-phthalimidooxyacetateHCID 12784561—

Reaction Steps

Bromoacetic acid (10.45 g) was dissolved in methanol (30 ml). To the solution was added an equivalent volume of diphenyl diazomethane in ethyl acetate at 45° C., and the reaction mixture was stirred at the same temperature for an hour. The solution was washed with 5% aqueous sodium bicarbonate and a saturated aqueous sodium chloride, and then dried over magnesium sulfate. The solution was evaporated in vacuo to give an oily product. This oil was dissolved in N,N-dimethylformamide (60 ml). To the solution was added N-hydroxyphthalimide (11.7 g) and triethylamine (15.1 ml), and the reaction mixture was stirred at ambient temperature for an hour. The resultant mixture was poured into a saturated aqueous sodium chloride (500 ml). The precipitates were collected by filtration, washed with water, and then dissolved in methylene chloride (700 ml). The solution was washed with a saturated aqueous sodium chloride, dried over magnesium sulfate, and then evaporated under reduced pressure to give benzhydryl 2-phthalimidooxyacetate (20.4 g), mp 173°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026695
Source datasetuspto-grants-1991_06
ORD IDord-0c4d89c9d79943d7b1e1b51d3c95c2b6
Source noteuspto-grants-1991_06