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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973335Generated: October 31, 2026

Hydrochloric Acid → 2-(2-Nitro-4-chlorophenoxy)benzyl alcohol

https://huagongshe.com/reaction/1973335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantBenzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)-HCID 11037—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(4-Chloro-2-nitrophenoxy)benzaldehydeHCID 15780312—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Nitro-4-chlorophenoxy)benzyl alcoholHCID 28945808—

Reaction Steps

10 Parts 2-(2-nitro-4-chlorophenoxy)benzaldehyde and 2.4 parts sodium cyanoborohydride is dissolved with stirring in a mixture of 22 parts of tetrahydrofuran, 20 parts methanol and 10 parts by volume 2,2,2-trifluoroethanol. To the resulting mixture is added a trace of methyl orange and a sufficient amount of 2 N hydrochloric acid in methanol to attain a deep red color. Stirring is continued for approximately 24 hours at which time the solvents are removed in vacuo. The red, oily residue is dissolved in water and ethyl ether, and the ether layer separated. The water layer is extracted three times with 18 parts portions of ethyl ether. The ether extracts are combined with the ether layer, and extracted once with 50 parts of water. The ether is removed in vacuo to give crude 2-(2-nitro-4-chlorophenoxy)benzyl alcohol which is purified by chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997401
Source datasetuspto-grants-1976_12
ORD IDord-ec2f41705d7e4c289484e9fe087899e4
Source noteuspto-grants-1976_12