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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1179060생성일: 2026년 10월 27일

1,2-Dichloroethane → N'-Benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine hydrochloride

https://huagongshe.com/reaction/1179060

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Acetic AcidHCID 176—
반응물Benzo(b)thiophen-5-amineHCID 288032—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
생성물N'-Benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine hydrochlorideHCID 69337854—
생성물N'-benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamineHCID 69337855—

반응 단계

300 mg 5-Aminobenzothiophene and 435 mg 4-dimethylamino-4-phenyl-cyclohexanone were dissolved in dry 1,2-dichloroethane (20 ml) under argon. Glacial acetic acid (2 mmol) and 600 mg sodium triacetoxyborohydride were added to this mixture and the mixture was stirred for 24 hours at RT. For working up, the reaction mixture was concentrated and the residue was adjusted to pH 11 with five molar sodium hydroxide solution. The alkaline phase was diluted with water (10 ml) and extracted with ethyl acetate (3×20 ml). The combined extracts were dried over sodium sulfate and filtered and the filtrate was concentrated. The crude product was chromatographed over silica gel with ethyl acetate/ethanol (1:1). 230 mg of the nonpolar diastereomer of N′-benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine were obtained as a white solid, from which the corresponding hydrochloride was precipitated with 1.85 M ethanolic hydrochloric acid (0.54 ml) in 2-butanone (8 ml) (243 mg; m.p. 155-157° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07276518B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-bc78de4c9cb84a019a9fe4c0ef171897
출처 메모uspto-grants-2007_10