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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1505289생성일: 2026년 10월 27일

Triethylamine → (S,E)-N-(8-(tert-Butyldiphenylsilyloxy)-2-methyloct-5-en-4-yl)-P,P-diphenylphosphinic amide

https://huagongshe.com/reaction/1505289

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Diphenylphosphinic chlorideHCID 73910—
반응물(S,E)-8-(tert-Butyldiphenylsilyloxy)-2-methyloct-5-en-4-amine hydrochlorideHCID 53248329—
용매Hydrochloric AcidHCID 313—
용매DichloromethaneHCID 6344—
생성물(S,E)-N-(8-(tert-Butyldiphenylsilyloxy)-2-methyloct-5-en-4-yl)-P,P-diphenylphosphinic amideHCID 67310501119.6%

반응 조건

온도0 °C

반응 단계

To a solution of the amine 7 (400 mg, 1.01 mmol) in dry DCM (7 mL) were added Et3N (0.44 mL, 3.13 mmol), and then a solution of diphenylphosphinic chloride (Ph2POCl, 0.22 mL, 1.11 mmol) in dry DCM (3 mL) at 0° C. After being stirred at 0° C. for 15 min, the reaction mixture was allowed to warm to rt and stirred for 4 h, then diluted with DCM and 10% HCl. The aqueous phase was extracted with DCM and the combined organic layers were washed with sat. NaHCO3, dried (MgSO4), filtered and concentrated in vacuo to afford 720 mg of the crude title compound as a pale yellow solidified oil, which was used for the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09216976B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-1f5751e5aee54f9096b6db438cecf4cb
출처 메모uspto-grants-2015_12