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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859216Generated: November 1, 2026

Tetrahydrofuran → HCID 17608004, compound

https://huagongshe.com/reaction/859216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68614531HCID 68614531—
SolventWaterHCID 962—
ProductHCID 17608004HCID 1760800485%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 7.12 g (20.7 mmol) of (RS)-1-[4-(4-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methyl ester in 10.3 ml of a solution of sodium hydroxide (1N) is prepared and tetrahydrofurane is added until a clear solution is obtained. The mixture is heated to 50° C. for 1 hour. For the working-up, the tetrahydrofurane is evaporated under reduced pressure. The white suspension obtained is diluted with water, then filtered. The white product is treated with toluene and evaporated under reduced pressure to remove most of the water. The azetropic distillation is repeated three times. There are obtained 5.78 g (85% of theory) of (RS)-1-[4-(4-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151111B2
Source datasetuspto-grants-2006_12
ORD IDord-e2d23dfd230e430ea84bd6ec1f033808
Source noteuspto-grants-2006_12