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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500286Generated: November 1, 2026

18-Crown-6 → (4S,5R)-tert-butyl 4-(fluoromethyl)-2,2-dimethyl-5-(4-(3-(methylsulfonylmethyl)isoxazol-5-yl)phenyl)oxazolidine-3-carboxylate

https://huagongshe.com/reaction/1500286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
ReactantSodium methanesulfinateHCID 2733271—
Reactant(4S,5R)-tert-butyl 4-(fluoromethyl)-2,2-dimethyl-5-(4-(3-((methylsulfonyloxy)methyl)isoxazol-5-yl)phenyl)oxazolidine-3-carboxylateHCID 86695496—
SolventAcetonitrileHCID 6342—
Product(4S,5R)-tert-butyl 4-(fluoromethyl)-2,2-dimethyl-5-(4-(3-(methylsulfonylmethyl)isoxazol-5-yl)phenyl)oxazolidine-3-carboxylateHCID 8671317277.5%

Reaction Steps

(4S,5R)-tert-butyl 4-(fluoromethyl)-2,2-dimethyl-5-(4-(3-((methylsulfonyloxy)methyl)isoxazol-5-yl)phenyl)oxazolidine-3-carboxylate (200 mg, 0.413 mmol), sodium methanesulfinate (100 mg, 0.83 mmol), and 18-crown-6 (23 mg, 0.08 mmol) in acetonitrile (8 mL) are stirred at room temperature for 16 hours then the mixture is concentrated and purified by column chromatography on silica gel eluting with a gradient of ethyl acetate/heptane to afford the title compound (150 mg). m/z (Cl) 469 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206126B2
Source datasetuspto-grants-2015_12
ORD IDord-71910439d9c0478b85da387d57d73c6b
Source noteuspto-grants-2015_12