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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | 2-Phenylbutyric Acid | HCID 7012 | — |
| Reactant | 2-Phenoxyethyl methanesulfonate | HCID 226499 | — |
| Product | 4-(2-Mesyloxyethoxy)phenyl benzylketone | HCID 86754572 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962743 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-f59c121cca844a8bb94b070a82da3b2e |
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| Source note | uspto-grants-1999_10 |
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