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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355213Generated: November 1, 2026

Water → HCID 66917418, compound

https://huagongshe.com/reaction/2355213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium SulfiteHCID 24437—
ReactantHCID 58869153HCID 58869153—
Reactant2-Methylpropan-2-ol--water (1/1)HCID 71401949—
CatalystHCID 178511488HCID 178511488—
Solventtert-ButanolHCID 6386—
ProductHCID 66917418HCID 66917418—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of potassium osmate dihydrate (1.19 mg, 0.0034 mmol), hydroquinidine (anthraquinone-1,4-diyl)diether (7.32 mg, 0.00851 mmol), potassium ferricyanide (843 mg, 2.55 mmol) and K2CO3 (357 mg, 2.55 mmol) in t-BuOH/H2O (3.5 mL/4.5 mL) was cooled to 0° C. and a solution of 4-benzenesulfonyl-2-bromo-1-but-3-enyl-benzene (299 mg, 0.851 mmol) in t-BuOH (1 mL) was added. The reaction was maintained at 0° C. for 18 hours, then Na2SO3 (0.68 g) was added at 0° C. The reaction was allowed to warm to room temperature and water was added. The mixture was extracted twice with EtOAc, and the combined extracts were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified via flash chromatography (hexane/EtOAc) to afford (R)-4-(4-benzenesulfonyl-2-bromo-phenyl)-butane-1,2-diol (193 mg) with 86% ee. Chiral column: Chiralpak AS analytical, hexane/isopropanol (75/25), 1.1 mL/min flow rate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754759B2
Source datasetuspto-grants-2010_07
ORD IDord-c9c4a5dc11b145b99e18afa44abca5f1
Source noteuspto-grants-2010_07