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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691341Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 59255198, compound

https://huagongshe.com/reaction/1691341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant1-Benzylsulfanyl-4-((E)-2-nitro-vinyl)-benzeneHCID 59255337—
SolventAcetic AcidHCID 176—
ProductHCID 59255198HCID 5925519897.8%

Reaction Steps

To a solution of 1-benzylsulfanyl-4-((E)-2-nitro-vinyl)-benzene (950 mg, 3.5 mmol) described in Manufacturing Example 205-1-3 in acetic acid (0.6 mL) and dimethyl sulfoxide (10 mL) was added sodium borohydride (212 mg, 5.6 mmol) while the internal temperature was held at 30° C. or lower, which was stirred for 30 minutes at room temperature. The mixture was cooled with ice water, water was added, which was stirred for another 30 minutes. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (936 mg). The title compound was used in the following reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-efd547e451794962a6f02de5e4f0fe4a
Source noteuspto-grants-2012_04