참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Bromostyrene | HCID 16263 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | Oxalic acid, di(2-phenylethyl) ester | HCID 6421929 | — |
| 촉매 | Tert-Butylhydroquinone | HCID 16043 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethylacetate heptane | HCID 21899848 | — |
| 생성물 | 2-Phenylethyl 2-oxo-2-(4-vinylphenyl)acetate | HCID 89488047 | 68.1% |
반응 단계
A Grignard reagent prepared from freshly distilled 4-bromostyrene (9.45 g, 51.6 mmol) and magnesium (1.31 g, 54.0 mmol) in THF (70 mL) was added dropwise to a stirred solution of bis(2-phenylethyl)oxalate (14.0 g, 46.9 mmol) in THF (120 mL) at −60° C. The mixture was left warming to room temperature, and then poured onto a mixture of ice (200 g) and a saturated solution of NH4Cl (200 mL). Extraction with diethyl ether (500 mL), washing with a saturated solution of NaCl (300 mL, 3×), re-extraction of the aqueous phase with ether, drying of the combined organic phases (Na2SO4), adding of tert-butyl hydroquinone (TBHQ, ca. 0.3 mg), concentrating and drying under vacuum (0.5 mbar, 0.5 h) afforded 19.40 g of the crude compound. Column chromatography (SiO2, heptane/ethyl acetate 98:2), adding of TBHQ (0.2 mg) to the product fractions, concentrating and drying under vacuum gave 8.95 g (68%) of the desired compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09315763B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-3655e4b7cb7a4ff4b844b76d4115d399 |
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| 출처 메모 | uspto-grants-2016_04 |
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