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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853172Generated: October 30, 2026

Water → HCID 11673685, compound

https://huagongshe.com/reaction/853172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroacetamideHCID 6580—
ReactantSodium hydrideHCID 24758—
ReactantSafinamide Impurity 8HCID 887902—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11673685HCID 116736855.1%

Reaction Steps

A solution of 500 mg of [4-(3-fluoro-benzyloxy)-phenyl]-methanol [Example 25b)] in 10 ml of tetrahydrofurane was treated at room temperature with 57 mg of sodium hydride (55% dispersion in oil) and stirred for 1 h. Thereafter, 183 mg of chloroacetamide were added and the mixture was heated to reflux for 48 h. For the working-up, the cooled mixture was treated with water and extracted with ethyl acetate. The organic layer was dried over magnesium sulphate and evaporated under reduced pressure. For purification, the crude material obtained was chromatographed on silica gel using a gradient of dichloromethane to a 4:1-mixture-mixture of dichloromethane and methanol as the eluent. After crystallisation from ether, there were obtained 29 mg (5% of theory) of 2-[4-(3-fluoro-benzyloxy)-benzyloxy]-acetamide as a white solid; MS: m/e=307 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253318B2
Source datasetuspto-grants-2007_08
ORD IDord-5211eaa6135b46b0b978df97490775d3
Source noteuspto-grants-2007_08