Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamate → 4-t-Butyloxycarbonylamino-3-hydroxy-6-methylhept-1-ene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | tert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamate | HCID 104275 | — |
| 반응물 | HCID 178418507 | HCID 178418507 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-t-Butyloxycarbonylamino-3-hydroxy-6-methylhept-1-ene | HCID 13856048 | — |
반응 단계
To a stirred 0° C. solution of Boc-leucinal (3.00 g, 13.9 mmol) in dry THF (70 ml) was added vinyl magnesium bromide (35 ml of a 1.0M solution in THF). After 5 hours, the mixture was quenched with 1.0M NH4Cl (50 ml). Most of the THF was evaporated in vacuo and the residue was extracted with ether several times. The combined extracts were washed (brine), dried (Na2SO4), filtered, and evaporated to give the desired product as a 3:2 mixture of hydroxydiastereomers in 65% field.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04725584 |
| 출처 데이터셋 | uspto-grants-1988_02 |
| ORD ID | ord-8bab05ee85f7428ab7f581565106fcda |
| 출처 메모 | uspto-grants-1988_02 |