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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891953Generated: November 3, 2026

Dimethyl Sulfoxide → 2-(4-Fluoro-benzyl)-5-(2-nitro-ethyl)-furan

https://huagongshe.com/reaction/1891953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-Fluoro-benzyl)-5-((E)-2-nitro-vinyl)-furanHCID 59255389—
SolventAcetic AcidHCID 176—
Product2-(4-Fluoro-benzyl)-5-(2-nitro-ethyl)-furanHCID 5925520293.5%

Reaction Steps

To a solution of 2-(4-fluoro-benzyl)-5-((E)-2-nitro-vinyl)-furan (1.21 g, 4.89 mmol) described in Manufacturing Example 208-1-3 in acetic acid (0.6 mL) and dimethyl sulfoxide (10 mL) was added sodium borohydride (296 mg, 7.82 mmol), which was stirred for 30 minutes at room temperature. The mixture was cooled with ice water and 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 (1.14 g). The title compound was used in the following reaction without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-29b99f41487c4acdabac8d72ba485095
Source noteuspto-grants-2013_08