돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41655생성일: 2026년 10월 26일

Amantadine → N-phenyladamantan-1-amine

https://huagongshe.com/reaction/41655

반응식

참여 물질

역할이름HCID투입량
반응물AmantadineHCID 2130—
반응물Diethyl EtherHCID 3283—
반응물BromobenzeneHCID 7961—
반응물Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
용매TolueneHCID 1140—
생성물N-phenyladamantan-1-amineHCID 30393965.7%

반응 단계

A mixture of Pd(dba)2 (0.259 g, 0.450 mmol) and (±)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthalene (0.417 g, 0.670 mmol) in toluene (40 mL) was stirred for 30 min at room temperature before adding 1-adamantylamine (2.269 g, 15.0 mmol), bromobenzene (1.60 mL, 15.2 mmol) and sodium tert-butoxide (2.02 g, 21.0 mmol). The reaction solution was stirred for 24 h at 100° C. After cooling the reaction mixture to room temperature, Et2O (50 mL) was added. The reaction mixture was filtered through a pad of celite and was concentrated. Flash column chromatography (silicagel, 7:1 hexanes/EtOAc) afforded the desired product (2.239 g, 65.7%) as a pale yellow solid. 1H NMR (300 MHz, CDCl3) δ 7.18 (t, J=7.6 Hz, 2H), 6.83 (m, 3H), 3.26 (br. s, 1H), 2.14 (m, 3H), 1.91 (m, 6H), 1.71 (m, 6H); 13C NMR (75 MHz, CDCl3) δ 146.3, 129.0, 119.4, 119.3, 52.5, 43.8, 36.8, 30.0. HRMS-ESI (m/z): [M+H]+ calcd for C16H21N, 228.1747. found, 228.1756.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530687B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-1d7816f6841345f49a67baf64ce4e240
출처 메모uspto-grants-2013_09