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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255985Generated: October 30, 2026

Benzyl Alcohol → HCID 13907841, compound

https://huagongshe.com/reaction/255985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
Reactant2-NitroanilineHCID 6946—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventZincchlorideHCID 3007855—
ProductHCID 13907841HCID 13907841—

Reaction Steps

To 20.4 parts of 36% w/w hydrochloric acid in which had previously been dissolved 13.4 parts of anhydrous zinc chloride are added 27.6 parts of o-nitro-aniline and 10.8 parts of benzyl alcohol. This mixture is stirred under reflux temperature for 6 hours and then poured into a hot solution of 50 parts of sodium hydroxide in 100 parts of water. After allowing the decomposed reaction mixtures to cool the organic phase is extracted with ether, and the ether solution washed with water, the ether evaporated and the residue distilled to give a fraction with boiling point 192°-8° C. at 0.4 millibars. This fraction after dilution with 40°-60° petroleum ether containing a little ether yields 4-benzyl-2-nitro-aniline m.p. 80°-3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04700003
Source datasetuspto-grants-1987_10
ORD IDord-a03f485509b64f8f921c20d7fcc3cdf6
Source noteuspto-grants-1987_10