Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 579514생성일: 2026년 10월 26일
Ethyl 2-(acetoxymethyl)-2-(tert-butoxycarbonylamino)hex-5-enoate → Ethyl 2-(acetoxymethyl)-2-(tert-butoxycarbonylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate
https://huagongshe.com/reaction/579514
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 2-(acetoxymethyl)-2-(tert-butoxycarbonylamino)hex-5-enoate | HCID 86663718 | — |
| 반응물 | HCID 178419189 | HCID 178419189 | — |
| 촉매 | 1,2-Bis(diphenylphosphino)ethane | HCID 74267 | — |
| 촉매 | Chloro(1,5-cyclooctadiene)iridium(I) dimer | HCID 6436381 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Ethyl 2-(acetoxymethyl)-2-(tert-butoxycarbonylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate | HCID 66832797 | 54% |
반응 단계
While under an argon atmosphere, a solution of chloro(1,5-cyclooctadiene)iridium(I) dimer (160 mg, 0.23 mmol) and 1,2-bis(diphenyl-phosphino) ethane (190 mg, 0.48 mmol) in dichloromethane (50 mL) was treated with pinacol borane (7.78 g, 61 mmol, 8.8 mL) and stirred for 15 minutes. To this mixture was added a solution of ethyl 2-(acetoxymethyl)-2-(tert-butoxycarbonylamino)hex-5-enoate (10 g, 30.4 mmol) in dichloromethane (50 mL). After stirring for 19 h at room temperature the solution was concentrated and purified using a combiflash system (120 g column, eluting with 5-50% ethyl acetate in heptanes) to give ethyl 2-(acetoxymethyl)-2-(tert-butoxycarbonylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexanoate (7.5 g, 54%). 1H NMR (CDCl3) δ 5.49 (bs, 1H), 4.72 (d, 1H), 4.33 (d, 1H), 4.23 (q, 2H), 2.18 (m, 1H), 2.01 (s, 3H), 1.69 (m, 2H), 1.43 (s, 9H), 1.29 (m, 4H), 1.23 (s, 12H), 0.88 (t, 3H), 0.74 (t, 2H). MS found for C22H40BNO8 m/z [480(M+Na)].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09040703B2 |
|---|
| 출처 데이터셋 | uspto-grants-2015_05 |
|---|
| ORD ID | ord-7a260365f3ba4007bc5b2e4979529296 |
|---|
| 출처 메모 | uspto-grants-2015_05 |
|---|