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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637303Generated: October 25, 2026

4-Allyloxybenzoyl chloride → 7-Methacryloyloxy-2-naphthyl 4-allyloxybenzoate

https://huagongshe.com/reaction/1637303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Allyloxybenzoyl chlorideHCID 11790137—
Reactant2,7-Naphthalenediol monomethacrylateHCID 54509337—
ReactantHydroquinone monomethacrylateHCID 69210285—
SolventTriethylamineHCID 8471—
Product7-Methacryloyloxy-2-naphthyl 4-allyloxybenzoateHCID 1934897295%

Reaction Steps

In the same way as described in Example 2, 29.5 g (0.15 mol) of 4-allyloxybenzoyl chloride and 34.5 g (0.15 mol) of 2,7-naphthalenediol monomethacrylate (obtainable in a manner similar to that of the hydroquinone monomethacrylate referred to in Example 2 of U.S. Pat. No. 4,604,342) were reacted with triethylamine as acid scavenger. 7-Methacryloyloxy-2-naphthyl 4-allyloxybenzoate, C22H20O5, with an m.p. of 85° C. was obtained in 95% yield. The 1,4-, 1,5- and 2,6-disubstituted naphthalene derivatives can be prepared in the same way.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040411
Source datasetuspto-grants-2000_03
ORD IDord-ddcdfa0a1195484184ec68d87137acf7
Source noteuspto-grants-2000_03