Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 337552생성일: 2026년 10월 24일
1,4-Bis(diphenylphosphino)butane → 1,1-Dimethylethyl cyclopropyl{[2,3-dichloro-5-(2-hydroxyethyl)phenyl]methyl}carbamate
https://huagongshe.com/ko/reaction/337552
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,4-Bis(diphenylphosphino)butane | HCID 82124 | — |
| 반응물 | Sodium Perborate | HCID 517072 | — |
| 반응물 | 4,4,5,5-Tetramethyl[1,3,2]dioxaborolane | HCID 2734768 | — |
| 반응물 | 1,1-Dimethylethyl cyclopropyl[(2,3-dichloro-5-ethenylphenyl)methyl]carbamate | HCID 66895414 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1,1-Dimethylethyl cyclopropyl{[2,3-dichloro-5-(2-hydroxyethyl)phenyl]methyl}carbamate | HCID 66897112 | — |
반응 단계
1,1-Dimethylethyl cyclopropyl[(2,3-dichloro-5-ethenylphenyl)methyl]carbamate (1 eq.) from the previous step, [Ir(COD)Cl]2 (0.025 eq.) and DPPB (0.05 eq.) were combined in THF (0.11 M). To this solution was then added 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.3 eq.) and the resulting red solution was stirred at RT for 12 h. Finally, sodium perborate (0.1 M aqueous solution, 1 eq.) was added and the now black biphasic solution was vigorously stirred at RT for another 12 h. The aqueous layer was separated and back-extracted with ether. The combined organic extracts were then washed further with 1 N aq. NaOH, water and brine. This was then dried over Na2SO4, filtered and the filtrate concentrated in vacuo to afford a pale yellow oil. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 9:1 (v/v) Hex:EtOAc→3:7 (v/v) EtOAc:Hex) afforded the title compound as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08889714B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-b146069054414e8eb218ee37d816b6d7 |
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| 출처 메모 | uspto-grants-2014_11 |
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