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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397201Generated: October 29, 2026

Sodium Sulfite → ethyl (3S)-3-{[(2-chloro-4-fluorophenyl)amino]sulfanyl}-3,6-dihydro-2H-pyran-4-carboxylate

https://huagongshe.com/reaction/1397201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
ReactantBenzenamine, 2-chloro-4-fluoro-HCID 75013—
ReactantTert-Butyl hypochloriteHCID 521297—
Reactantethyl (3S)-3-sulfanyl-3,6-dihydro-2H-pyran-4-carboxylateHCID 86676958—
SolventDichloromethaneHCID 6344—
Productethyl (3S)-3-{[(2-chloro-4-fluorophenyl)amino]sulfanyl}-3,6-dihydro-2H-pyran-4-carboxylateHCID 86676959—

Reaction Steps

To a solution (400 mL) of ethyl (3S)-3-sulfanyl-3,6-dihydro-2H-pyran-4-carboxylate (14.5 g) in dichloromethane was added dropwise tert-butyl hypochlorite (10 mL) at −78° C. After stirring for 30 min, 2-chloro-4-fluoroaniline (23 mL) was added dropwise at −78° C. The reaction mixture was stirred for 1 hr, and the reaction was discontinued with 5% aqueous sodium sulfite solution (300 mL). After extraction with dichloromethane (300 mL), the extract was washed with water, and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography (hexane/ethyl acetate=15:1→5:1) to give the title compound as a crude product (20.0 g, 96.3% ee). This product was crystallized from diisopropyl ether/hexane (120 mL, 1:5) to give the title compound (12.3 g, 62%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901171B2
Source datasetuspto-grants-2014_12
ORD IDord-8514da31e6444de3a83629c5f963cc04
Source noteuspto-grants-2014_12