참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | m-Chlorostyrene | HCID 14905 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (R)-(+)-3-Chlorostyrene oxide | HCID 10898919 | 92% |
반응 단계
A 2-necked round-bottom flask equipped with a water-cooled overhead stirrer was charged with 3-chlorostyrene (5.01 g, 3.61×10−2 mol), CH2Cl2 (45 mL), (R,R)-3 (0.578 g, 9.10×10−4 mol), and 4-PPNO (0.924 g, 5.40×10−3 mol). The solution was cooled to 0° C., and precooled buffered bleach (0.6 M, 75 mL, 4.50×10−2 mol, Clorox®, buffered to pH=11.3 with 0.05 M Na2HPO4 and 1M NaOH) was added. The two phase system was stirred vigorously, and the course of the reaction was monitored by GC. Upon complete consumption of starting olefin (<6 h), the reaction mixture was filtered through a plug of Celite on a coarse glass frit and washed with CH2Cl2 (75 mL). The organic layer of the filtrate was washed with distilled water (2×25 mL), and the aqueous layers were extracted with CH2Cl2 (2×25 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo. Removal of the catalyst was effected by elution through a pad of SiO2 (30 g) using pentane and CH2Cl2 (1:1). The eluent was concentrated in vacuo, and subsequent bulb-to-bulb distillation (70° C., 0.6 mm Hg) from CaH2 afforded (R)-3-chlorostyrene oxide (5.15 g, 92%) as a pale yellow liquid in 32% ee.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06800766B2 |
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| 출처 데이터셋 | uspto-grants-2004_10 |
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| ORD ID | ord-663f8e6a1b424d92b94717adaa260966 |
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| 출처 메모 | uspto-grants-2004_10 |
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