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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891740Generated: October 30, 2026

Acetic Acid → 1-Cyclohexyloxy-4-(2-nitro-ethyl)-benzene

https://huagongshe.com/reaction/1891740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59255256HCID 59255256—
SolventDimethyl SulfoxideHCID 679—
Product1-Cyclohexyloxy-4-(2-nitro-ethyl)-benzeneHCID 5925508244.4%

Reaction Steps

To an acetic acid (3.3 mL) and dimethyl sulfoxide (55 mL) solution of 1-cyclohexyloxy-4-((E)-2-nitro-vinyl)-benzene (3.3 g, 13.1 mmol) described in Manufacturing Example 79-1-2 was added sodium borohydride (793 mg, 21 mmol) at room temperature while cooling appropriately. This mixture was stirred for 1 hour 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=4:1) to obtain the title compound (1.45 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-55f12e44a77f499ba01caddc5d5c3fdd
Source noteuspto-grants-2013_08