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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691018Generated: November 1, 2026

Acetic Acid → 2-Methyl-5-(4-(2-nitro-ethyl)-benzyl)-furan

https://huagongshe.com/reaction/1691018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furanHCID 59255436—
SolventWaterHCID 962—
Product2-Methyl-5-(4-(2-nitro-ethyl)-benzyl)-furanHCID 5925552777%

Reaction Steps

To a mixture of 2-methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furan (120 mg) described in Manufacturing Example 46-1-4, acetic acid (0.2 mL) and dimethyl sulfoxide (3.4 mL) was added sodium borohydride (29 mg, 0.77 mmol) at room temperature while cooling appropriately, which was stirred for 20 minutes at room temperature. Water was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue was purified by neutral silica gel column chromatography (ethyl acetate:heptane=1:5) to obtain the title compound (90 mg, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-8919e501354d45b88e16bc6836fa3d24
Source noteuspto-grants-2012_04