참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyl methyl ether | HCID 12338 | — |
| 반응물 | Triethyl phosphite | HCID 31215 | — |
| 반응물 | Benzaldehyde, 4-(phenylmethoxy)- | HCID 78109 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | tert-Butanol | HCID 6386 | — |
| 생성물 | Ethyl 3-[4-(benzyloxy)phenyl]-2-ethoxyprop-2-enoate | HCID 54423854 | 92% |
반응 단계
P(OEt)3 was added dropwise to a mixture of tent-butyl methyl ether 55 mL) and potassium tert-butoxide (4.65 g, 41.4 mmol) under a nitrogen atmosphere at 20-30° C. 4-Benzyloxybenzaldehyde (4.61 g, 21.7 mmol) was added in portions to this mixture at 5° C. followed by the addition of tert-butyl alcohol (6.70 g). The reaction mixture was allowed to reach 15° C. and stirred at this temperature for approximately 30 min, after which the reaction was completed (as judged by TLC). Water (30 mL) was added at 5-10° C., and the phases were allowed to separate. The organic phase was concentrated in vacuo, and ethanol (30 mL) was added to the stirred solution. After crystallization had occurred, water (18 mL) was added to the suspension. The light-yellow title compound was filtered off, washed with ethanol/water (1:1 v/v), and dried in vacuo to yield 6.52 g (92% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08513233B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-61d528ca74cd4b48a02921468bcf1878 |
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| 출처 메모 | uspto-grants-2013_08 |
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