Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11900생성일: 2026년 10월 24일
2-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanol → 2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochloride
https://huagongshe.com/ko/reaction/11900
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-(4-Amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanol | HCID 9997789 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2-(4-Amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochloride | HCID 9997788 | 80% |
반응 단계
1.0 g of 2-(4-amino-3-chloro-5-trifluoromethylphenyl)-2-tert-butylaminoethanol was dissolved in 20 ml of diethyl ether and filtered. Saturated solution of hydrogen chloride in isopropanol was added dropwise and acidified to pH=2. The precipitate was collected by filtration, washed with anhydrous ether, and dried to give crude 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochloride. The crude product was dissolved in absolute ethanol at a ratio of 1:5 w/v. Filtered, anhydrous ether was added dropwise until small amount of crystals was precipitated. Lyophilized and filtered to give 2-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-2-tert-butylaminoethanol hydrochloride. Yield 80–90%; melting point 205–206° C. (dec). 1H-NMR (DMSO-d6) δ:1.24 (9H, s), 3.77(2H, d), 4.42–4.44(1H, m), 7.72(1H, s), 7.87(1H, s).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07098364B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-b0b6eaf0998a4f67af847dbabab1ce48 |
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| 출처 메모 | uspto-grants-2006_08 |
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