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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993094Generated: October 30, 2026

Methanol → 3-Hydroxybenzyl alcohol

https://huagongshe.com/reaction/1993094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantTetrahydrofuranHCID 8028—
ReactantImidazolateHCID 3386966—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Product3-Hydroxybenzyl alcoholHCID 102—

Reaction Steps

Scheme 20 Example 4 illustrates the preparation of carbamates in which an alkyloxycarbonylimidazole 20.8 is employed. In this procedure, a carbinol 20.5 is reacted with an equimolar amount of carbonyl diimidazole 20.11 to prepare the intermediate 20.8. The reaction is conducted in an aprotic organic solvent such as dichloromethane or tetrahydrofuran. The acyloxyimidazole 20.8 is then reacted with an equimolar amount of the amine R′NH2 to afford the carbamate 20.7. The reaction is performed in an aprotic organic solvent such as dichloromethane, as described in Tet. Lett., 42, 2001, 5227, to afford the carbamate 20.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649015B2
Source datasetuspto-grants-2010_01
ORD IDord-6a12d46094a14aa391fcdd7a55de09dd
Source noteuspto-grants-2010_01