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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091239Generated: October 29, 2026

Acetic Acid → HCID 59713390, compound

https://huagongshe.com/reaction/1091239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantNitrocyclohexaneHCID 14285—
Reactant3,5-DichlorobenzaldehydeHCID 35746—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 59713390HCID 59713390—

Reaction Steps

25% sodium methoxide solution (24.9 mmol, 5.7 mL) was diluted with methanol (40 mL), cooled in an ice bath, and nitrocyclohexane was added dropwise over 10 min. The mixture was stirred for 30 min, cooled in an ice bath, and solid 3,5-dichlorobenzaldehyde was added. The mixture was stirred over the weekend, recooled in an ice bath, and treated with 2 mL of glacial acetic acid. The mixture was poured into water (125 mL) and extracted with ether (2×75 mL). The combined ether extracts were washed with water (100 mL) and dried over MgSO4. Removal of the solvent left crude (3,5-dichloro-phenyl)-(1-nitro-cyclohexyl)-methanol (8.93 g) as a yellow oil. Flash chromatography on silica gel, eluting with a 0-100% ether in hexanes gradient provided product of increased purity (ca. 70%). 1H NMR (500 MHz, CDCl3) δ (ppm): 7.35 (s, 1H), 7.19 (s, 2H), 4.90 (s, 1H), 0.9-1.8 (m, 10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129355B2
Source datasetuspto-grants-2012_03
ORD IDord-efd9a7c3294e4116a92d3eea12526b10
Source noteuspto-grants-2012_03