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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714824Generated: November 2, 2026

Ethanethiol → HCID 68575388, compound

https://huagongshe.com/reaction/1714824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantBoron trifluoride etherateHCID 8000—
ReactantHCID 68574648HCID 68574648—
SolventDichloromethaneHCID 6344—
ProductHCID 68575388HCID 68575388—

Reaction Steps

A solution of 139.8 mg of benzyl 4-[4-(5-bromopyrimidin-2-yloxy)phenyl]-3-hydroxy-5-[4 -(3-methoxypropyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]piperidine-1-carboxylate in 0.5 ml of dichloromethane is added to a mixture of 0.232 ml of boron trifiuoride etherate and 0.4 ml of ethanethiol. The reaction mixture is stirred at room temperature under argon for 20 hours. The solvent is then evaporated off, and 2 ml of water are added to the residue. The aqueous phase is extracted three times with 5 ml of ethyl acetate each time. The combined organic phases are dried with sodium sulphate, filtered and evaporated. The title compound is obtained as a beige wax from the residue by flash chromatography (SiO2 60F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799779B2
Source datasetuspto-grants-2010_09
ORD IDord-893df30155474e6a8cc39cf51489f9bd
Source noteuspto-grants-2010_09