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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362421Generated: October 30, 2026

Sodium Hydroxide → HCID 86673443, compound

https://huagongshe.com/reaction/2362421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl carbamateHCID 77922—
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantHCID 86673442HCID 86673442—
SolventWaterHCID 962—
Solvent1-PropanolHCID 1031—
ProductHCID 86673443HCID 86673443—

Reaction Conditions

Temperature0 °C

Reaction Steps

To tert-butyl carbamate (214 mg, 1.827 mmol) in n-propanol (1.75 mL) was added sodium hydroxide (71.3 mg, 1.784 mmol) in water (3.5 mL) followed by tert-butyl hypochlorite (0.201 mL, 1.78 mmol). After 5 min, the solution was cooled to 0° C. and treated with a solution of DHQD2(PHAL) (23.7 mg, 0.030 mmol) in n-propanol (1.75 mL). The reaction was diluted with n-propanol (3.5 mL), and treated with (E)-6-bromo-3-fluoro-2-styrylpyridine (121 mg, 0.435 mmol) as a solid in one portion. To this was added potassium osmate dihydrate (8.01 mg, 0.022 mmol) as a solid in one portion. The reaction was allowed to gradually warm to room temperature in the dewar overnight. The reaction was cooled to 0° C. and quenched by addition of sodium thiosulfate (150 mg) in water (3 mL). The ice bath was removed and stirring continued for 30 min. The reaction was diluted with ether, washed with water (3×), then brine, dried over magnesium sulfate, and concentrated. Column chromatography (25% EtOAc/Hex) gave 208 mg (quant.). Mass spec.: 411.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691821B2
Source datasetuspto-grants-2014_04
ORD IDord-57b4c05cbdbf49b1b07d3f4214f97463
Source noteuspto-grants-2014_04