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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364856Generated: November 1, 2026

1-(4-Bromophenyl)-2-{[2-(4-bromophenyl)-2-oxoethyl]thio}ethan-1-one → 2,2'-Sulfanediylbis[1-(4-bromophenyl)ethan-1-ol]

https://huagongshe.com/reaction/2364856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)-2-{[2-(4-bromophenyl)-2-oxoethyl]thio}ethan-1-oneHCID 290034—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product2,2'-Sulfanediylbis[1-(4-bromophenyl)ethan-1-ol]HCID 57346026—

Reaction Steps

To a solution of Example 159A (5.0 g, 11.68 mmol) in ethanol (78 mL) was added sodium borohydride (0.972 g, 25.7 mmol) portionwise and the mixture was stirred at room temperature for 20 minutes. Afterwards the solution was concentrated, then a solution of 1N aqueous hydrochloric acid (100 mL) was added and extracted with EtOAc. The organic extract was dried, filtered and concentrated to 5.05 g (100%) of a colorless solid as the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691938B2
Source datasetuspto-grants-2014_04
ORD IDord-5881965b546d430e8fd512201cb350f2
Source noteuspto-grants-2014_04