Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218251생성일: 2026년 10월 25일
Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromide → 4-Bromo-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzene
https://huagongshe.com/reaction/218251
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromide | HCID 370917 | — |
| 반응물 | HCID 60130680 | HCID 60130680 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | 4-Bromo-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzene | HCID 60130672 | 55.9% |
반응 단계
A suspension of 3,4,5-trimethoxybenzyltriphenylphosphonium bromide (1.69 g, 3.23 mmol) in tetrahydrofuran (30 mL) was cooled to 0° C. and butyllithium (2 mL of a 1.6 N solution in hexane, 3.23 mmol) was added dropwise. The brick red solution was stirred at 0° C. for 20 min, then a solution of 19 (0.96 g, ca 2.2 mmol) in tetrahydrofuran (12 mL) was added dropwise. The temperature was allowed to rise to room temperature overnight, than the reaction was diluted with tert-butylmethyl ether (ca 100 mL) and washed with water (ca 50 mL, containing 1 mL 2N HCl) then brine (30 mL). The organic layer was dried over sodium sulphate and the solvent removed under reduced pressure to give a crude which was purified by column (elution with cyclohexane:AcOEt 10:1) to give 0.75 g of 20 still impure with 20% of the E isomer.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08198302B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-ae5a82024ead43189050401038470273 |
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| 출처 메모 | uspto-grants-2012_06 |
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