Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757471Generated: November 3, 2026

Benzyl Bromide → 3-Benzyloxy-4-(1-adamantyl)benzoic acid

https://huagongshe.com/reaction/1757471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantMethyl 3-benzyloxy-4-(1-adamantyl)benzoateHCID 19387981—
Product3-Benzyloxy-4-(1-adamantyl)benzoic acidHCID 17867034—

Reaction Steps

18 g (63 mM) of the ester obtained in Example 9(a) are treated with benzyl bromide under the conditions described in Example 5(a) to lead, after the same treatment, to 17.5 g (74%) of methyl 3-benzyloxy-4-(1-adamantyl)benzoate. The derivative obtained is then saponified under the conditions described in Example 7(b) to lead, after the same treatment, to 13.6 g (96.6%) of the expected derivative, of melting point 240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446059
Source datasetuspto-grants-1995_08
ORD IDord-cdab5e5c805e496ca49a6b779eea4dea
Source noteuspto-grants-1995_08