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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78247Generated: October 29, 2026

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

https://huagongshe.com/reaction/78247

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 numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-3044b7c584c04644b3e310843ba90465
Source noteuspto-grants-2014_09