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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867325Generated: November 2, 2026

Sodium Chloride → 7-benzyloxy-5-oxiranyl-1H-quinolin-2-one

https://huagongshe.com/reaction/1867325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
ReactantLithium borohydrideHCID 4148881—
Reactant7-(Benzyloxy)-5-(chloroacetyl)quinolin-2(1H)-oneHCID 21072859—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product7-benzyloxy-5-oxiranyl-1H-quinolin-2-oneHCID 57469371—

Reaction Steps

Lithium borohydride (434 mg, 19.93 mmol) is added to a suspension of 7-benzyloxy-5-(2-chloroacetyl)-1H-quinolin-2-one (6 g, 18.31 mmol) in THF (150 mL) at 0° C.-5° C. and the mixture is stirred for 30 minutes. 2.5 N sodium hydroxide solution (43 mL, 107.50 mmol) is added and the mixture is stirred for 2 hours at 5° C.-10° C. and for 2.5 hours at ambient temperature. Then the reaction mixture is slowly combined with glacial acetic acid (6.5 mL) followed by semisaturated sodium chloride solution (100 mL) and stirred for a further 5 minutes. The precipitate formed is filtered off and the aqueous phase is extracted with ethyl acetate/THF (1/1.5×100 mL). The solid filtered off and the organic phases are combined, dried with sodium sulfate, and evaporated down. The crude product is stirred with methanol (30 mL) and the precipitate is filtered off and dried at ambient temperature. Yield: 4.8 g (89%); mass spectroscopy: [M+H]+=294.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632834B2
Source datasetuspto-grants-2009_12
ORD IDord-535023d492b247c29ce7da4aa062d9ef
Source noteuspto-grants-2009_12