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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236066Generated: October 26, 2026

Hydrochloric Acid → alpha-Methyl-3-nitrobenzenemethanol

https://huagongshe.com/reaction/236066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant3-Nitrophenylacetic acidHCID 15876—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
SolventMethanolHCID 887—
Productalpha-Methyl-3-nitrobenzenemethanolHCID 223135—

Reaction Conditions

Temperature25 °C

Reaction Steps

40 g of 3-nitrophenylacetic acid was added to a solution of 26 ml of 10M borane-methyl sulfide in 200 ml of THF, and the mixture was stirred at 25° C. for 3 hr. The solution was then acidified with HCl in methanol, followed by evaporation of the solvent. The product 3-nitrophenylethanol (IV, A=H) was partitioned between diethyl ether (Et2O) and aqueous sodium carbonate, and the Et2O layer dried over sodium sulfate. Evaporation of the Et2O afforded 34.8 g of 3-nitrophenylethanol (IV, A=H) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642378
Source datasetuspto-grants-1987_02
ORD IDord-091978e79fea444b8caf8f27f8199d7c
Source noteuspto-grants-1987_02