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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738618Generated: October 25, 2026

Phenylacetic Acid → 4-(2-Mesyloxyethoxy)phenyl benzylketone

https://huagongshe.com/reaction/1738618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetic AcidHCID 999—
Reactant2-Phenylbutyric AcidHCID 7012—
Reactant2-Phenoxyethyl methanesulfonateHCID 226499—
Product4-(2-Mesyloxyethoxy)phenyl benzylketoneHCID 8675457280%

Reaction Conditions

Temperature25 °C

Reaction Steps

The oil comprising 2-Phenoxyethyl methanesulfonate was prepared as described above in Example 1. The acylation and workup procedure was identical to that of Example 1 with the exception that 30.26 g (220 mmol) 2-phenylacetic acid was reacted instead of the 2-phenylbutyric acid. The organic layer obtained by the workup procedure was cooled to 25° C. and stirred at this temperature for 1 hour. The resulting crystallized product was filtered, washed with toluene and dried under vacuum at 40° C. to yield 53.18 g (159 mmol) of the 4-(2-mesyloxyethoxy)phenyl benzylketone as a tan colored solid. Yield: 80% on 2-phenoxyethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962743
Source datasetuspto-grants-1999_10
ORD IDord-f59c121cca844a8bb94b070a82da3b2e
Source noteuspto-grants-1999_10