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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5542생성일: 2026년 10월 23일

Triethylamine → 2,2,2-Trichloroethyl (+/-)-[2-(3',4'-dihydro-2'-hydroxyspiro[cyclopentane-1,1'(2'H)-naphthalen]-2'-yl)ethyl]carbamate

https://huagongshe.com/ko/reaction/5542

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,2,2-Trichloroethyl chloroformateHCID 87063—
반응물(+/-)-2'-(2-Aminoethyl)-3',4'-dihydrospiro[cyclopentane-1,1'(2'H)-napthalen]-2'-olHCID 19983233—
용매DichloromethaneHCID 6344—
생성물2,2,2-Trichloroethyl (+/-)-[2-(3',4'-dihydro-2'-hydroxyspiro[cyclopentane-1,1'(2'H)-naphthalen]-2'-yl)ethyl]carbamateHCID 5706702978.1%

반응 조건

온도0 °C

반응 단계

A solution of the product from Example 9 (0.88 g, 3.59 mmol) and triethylamine (0.40 g, 3.78 mmol) in 10 mL of CH2Cl2 was cooled to 0° C. and treated dropwise with 2,2,2-trichloroethylchloroformate (0.80 g, 3.78 mmol) in 2 mL CH2Cl2. The resulting solution was stirred at 0° C. for 30 minutes and warmed to room temperature. The reaction mixture was washed with saturated aq. NaHCO3 solution (10 mL). The aqueous phase was extracted with CH2Cl2 (10 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by chromatography (silica gel, 10:1 heptane/ethyl acetate) to give the title compound (1.18 g, 78%) as a viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245028
출처 데이터셋uspto-grants-1993_09
ORD IDord-01efe08bb86845ba8cb6c06c77c689fa
출처 메모uspto-grants-1993_09