Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640235Generated: October 25, 2026

Acetic Acid → 1-Benzyloxy-3-(2-nitro-ethyl)-benzene

https://huagongshe.com/reaction/640235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Benzyloxy-trans-beta-nitrostyreneHCID 5368282—
SolventDimethyl SulfoxideHCID 679—
Product1-Benzyloxy-3-(2-nitro-ethyl)-benzeneHCID 5925520557%

Reaction Steps

To an acetic acid (5.5 mL) and dimethyl sulfoxide (94 mL) solution of 1-benzyloxy-3-((E)-2-nitro-vinyl)-benzene (5.5 g, 21.5 mmol) described in Manufacturing Example 61-1-2 was added sodium borohydride (1.3 g, 34.4 mmol) at room temperature while cooling appropriately. This mixture was stirred for 1.5 hours at room temperature. 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, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1-4:1) to obtain the title compound (3.14 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-f3312406b5254db9a4b4b5865306b900
Source noteuspto-grants-2010_04