돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434339생성일: 2026년 10월 25일

Sodium hydride → 1-t-Butoxycarbonylmethyl-3-bromoperhydroazocin-2-one

https://huagongshe.com/reaction/434339

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-Bromoazocan-2-oneHCID 567205—
반응물Tert-butyl 2-iodoacetateHCID 11021060—
용매TetrahydrofuranHCID 8028—
생성물1-t-Butoxycarbonylmethyl-3-bromoperhydroazocin-2-oneHCID 13188852—

반응 단계

To a vigorously stirred suspension of 0.55 g sodium hydride in 30 ml tetrahydrofuran add over 20 min. a solution of 5.0 g t-butyl iodoacetate and 4.12 g 3-bromoperhydroazocin-2-one [Nagasawa et al., J. Med. Chem., 14 501 (1971)] dissolved in 35 ml tetrahydrofuran. After the addition is completed stir the reaction at room temperature for 1.5 hours then quench by the addition of 5-6 ml of saturated NH4Cl solution. Filter the reaction and concentrate the filtrate. Add ether to the residue, filter and wash the filtrate with H2O and brine. Dry the ether solution and concentrate to obtain 1-t-butoxycarbonylmethyl-3-bromoperhydroazocin-2-one. Prepare an analytical sample by silica gel chromatography. M.p. 107.5-109. Anal. (C13H22BrNO3). Calc: C, 48.75; H, 6.93; N, 4.37. Found: C, 48.78; H, 7.12; N, 4.26.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04396616
출처 데이터셋uspto-grants-1983_08
ORD IDord-df64c936db6c430aa36a96caf445b484
출처 메모uspto-grants-1983_08