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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765319Generated: November 1, 2026

Benzyl Alcohol → HCID 21107062, compound

https://huagongshe.com/reaction/1765319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPyridineHCID 1049—
ReactantHCID 21107064HCID 21107064—
SolventBenzeneHCID 241—
ProductHCID 21107062HCID 2110706241.8%

Reaction Steps

A solution of 3-isocyanato-1-oxo-1,2,3,4-tetrahydronaphthalene (10 g), benzyl alcohol (7.3 g), dry pyridine (3 mL), and benzene (50 mL) was refluxed for 90 min. At the conclusion of this period, the solution was cooled to room temperature, diluted with benzene (150 mL), and then washed with 5% aqueous hydrochloric acid solution (60 mL twice). The organic layer was dried and evaporated under vacuum to yield a residue. The residue was crystallized by dissolving in benzene (35 mL) and diluting with petroleum ether (25 mL). Crystals thus obtained were recrystallized in the same manner to obtain the title compound (6.6 g, mp 79.5–81.5° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226942B2
Source datasetuspto-grants-2007_06
ORD IDord-9391ddc514104731a9cb2994a2994cfb
Source noteuspto-grants-2007_06