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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477375Generated: October 29, 2026

Ethyl Thioglycolate → HCID 54250288, compound

https://huagongshe.com/reaction/477375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantSodium hydrideHCID 24758—
Reactant2-BromomethylnaphthaleneHCID 70320—
ReactantEthyl (4-methylbenzylthio)acetateHCID 4107274—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54250288HCID 54250288—

Reaction Steps

The procedure is as in Example 29 for the preparation of ethyl (4-methylbenzylthio)acetate, starting with 2-bromomethylnaphthalene (20 g), sodium hydride (5.1 g) in a 50% strength dispersion in liquid paraffin and ethyl 2-mercaptoacetate (10.9 g) in tetrahydrofuran (200 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (80:20 by volume) as eluent, ethyl (2-naphthylmethylthio)acetate (12 g) is obtained, and is used in the crude state in the subsequent syntheses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886835
Source datasetuspto-grants-1989_12
ORD IDord-50cdf81e43c54a4cb1d2f95816c908bf
Source noteuspto-grants-1989_12