참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenylacetic Acid | HCID 999 | — |
| 반응물 | 2-Phenylbutyric Acid | HCID 7012 | — |
| 반응물 | 2-Phenoxyethyl methanesulfonate | HCID 226499 | — |
| 생성물 | 4-(2-Mesyloxyethoxy)phenyl benzylketone | HCID 86754572 | 80% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05962743 |
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| 출처 데이터셋 | uspto-grants-1999_10 |
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| ORD ID | ord-f59c121cca844a8bb94b070a82da3b2e |
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| 출처 메모 | uspto-grants-1999_10 |
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