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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614236Generated: November 2, 2026

2-Bromomethylnaphthalene → HCID 19773009, compound

https://huagongshe.com/reaction/1614236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromomethylnaphthaleneHCID 70320—
ReactantHCID 14899758HCID 14899758—
ProductHCID 19773009HCID 1977300995%

Reaction Steps

2-Bromomethylnaphthalene was reacted with 2-allyloxy-3-hydroxybenzaldehyde using the conditions described in Example 1 to give 2-allyloxy-3-(naphth-2-ylmethoxy)benzaldehyde as an oil in 95% yield. A mixture of the product so obtained (1.3 g), p-toluenethiol (0.8 g), sodium hydride (55% w/w dispersion in oil, 0.28 g) and dimethylformamide (10 ml) was heated to 100° C. for 1.3 hours. The mixture was partitioned between ethyl acetate and water. The organic layer was washed with water, dried (MgSO4) and evaporated. The residue was purified by column chromatography using a 4:1 v/v mixture of methylene chloride and ethyl acetate as eluent. There was thus obtained 2-hydroxy-3-(naphth-2-ylmethoxy)benzaldehyde (0.7 g), m.p. 105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196422
Source datasetuspto-grants-1993_03
ORD IDord-17432b83691e40fda8f78c79267bd022
Source noteuspto-grants-1993_03