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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158678Generated: November 3, 2026

Phosphate → [2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1158678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantSodium HydroxideHCID 14798—
Reactant4-FluorostyreneHCID 67883—
Reactanttert-Butyl carbamateHCID 77922—
ReactantTert-Butyl hypochloriteHCID 521297—
CatalystPotassium osmate(VI) dihydrateHCID 53393272—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product[2-(4-Chloro-phenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl esterHCID 16244250—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of carbamic acid tert-butyl ester (0.22 g) in acetonitrile (6 mL) was added in sequence at 0° C.: Sodium hydroxide (52 mg) in water (5 mL); after 2 minutes tert-butyl hypochlorite (139 mL); after 10 minutes potassium osmate(VI) dihydrate (9 mg) in water (1 mL); after 1 minute hydroquinine (anthraquinone-1,4-diyl)diether (26 mg) in acetonitrile (4 mL); after 3 minutes acetonitrile (6.7 mL) and phosphate buffer (3.3 mL, 0.5 M pH 7.65); after 5 minutes enough sodium biphosphate monohydrate to make pH=7.65; and finally 4-fluorostyrene. The reaction was quenched after stirring 3 hours at 25° C. with sodium sulfite (0.20 g) in water (2 mL) at 0° C. The phases were separated and the aqueous layer extracted with ethyl acetate (3×20 mL). The combined organic phases were washed with water

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812023B2
Source datasetuspto-grants-2010_10
ORD IDord-2af17e0e69b84991ae1437bf54fcdcac
Source noteuspto-grants-2010_10