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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419896Generated: November 4, 2026

Hydrochloric Acid → (6-Chloronaphthalen-2-yl)methanol

https://huagongshe.com/reaction/2419896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantMethyl 6-chloro-2-naphthoateHCID 13384252—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product(6-Chloronaphthalen-2-yl)methanolHCID 1338425398%

Reaction Steps

A solution of the methyl 6-chloro-2-naphthoate (111 g.) in ether (2.5 1.) is added, dropwise below 25° C. under nitrogen, to a stirred mixture of ether (250 ml.) and a 70% solution (250 ml.) of sodium dihydro-bis-(2-methoxyethoxy)aluminate in benzene during 1 hour. The mixture is stirred for a further 30 minutes and 2N-hydrochloric acid (250 ml.) is added cautiously. The solution is decanted from undissolved solid, and concentrated hydrochloric acid is added to the solid until it dissolves. The two solution thus obtained are combined, and ether (1 l.) and a mixture of ice and water (1 l.) are added. The ethereal layer is separated, and the aqueous phase extracted with ether. The ethereal solutions are combined, washed with water, dried and evaporated to give 6-chloro-2-hydroxymethylnaphthalene (95 g.) which may be further purified by crystallisation from toluene to give material of m.p. 134°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107329
Source datasetuspto-grants-1978_08
ORD IDord-2cc89c1d62a44c6980fb0dd0bc2023fd
Source noteuspto-grants-1978_08