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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614239Generated: October 30, 2026

Allyl bromide → HCID 19773037, compound

https://huagongshe.com/reaction/1614239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantBenzoic acid, 3,5-dihydroxy-, ethyl esterHCID 20098—
Reactant2-BromomethylnaphthaleneHCID 70320—
ProductHCID 19773037HCID 1977303715%

Reaction Steps

Ethyl 3,5-dihydroxybenzoate was reacted in turn with 2-bromomethylnaphthalene and allyl bromide using the conditions described in Example 1 to give ethyl 5-allyloxy-3-(naphth-2-ylmethoxy)benzoate in 15% yield, as an oil. Following the procedures described in the portion of Example 3 which is concerned with the preparation of starting materials the product so obtained was reacted with thiazol-2-yl-lithium to give 5-allyloxy-3-(naphth-2-ylmethoxy)phenyl 2-thiazolyl ketone in 52% yield, m.p. 65°-67° C., and that product was reacted with ethylmagnesium to give the required starting material in 49% yield, as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196422
Source datasetuspto-grants-1993_03
ORD IDord-978a2252105a4688baa9f58642802d57
Source noteuspto-grants-1993_03