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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Benzenamine, 2-chloro-4-fluoro- | HCID 75013 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | ethyl (3S)-3-sulfanyl-3,6-dihydro-2H-pyran-4-carboxylate | HCID 86676958 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl (3S)-3-{[(2-chloro-4-fluorophenyl)amino]sulfanyl}-3,6-dihydro-2H-pyran-4-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901171B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-8514da31e6444de3a83629c5f963cc04 |
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| Source note | uspto-grants-2014_12 |
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