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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 925105생성일: 2026년 10월 26일

(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine → 1,1,3-Trimethylindan-4-amine

https://huagongshe.com/reaction/925105

반응식

참여 물질

역할이름HCID투입량
반응물(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amineHCID 14535936—
반응물HCID 178418361HCID 178418361—
촉매HCID 178418390HCID 178418390—
용매TolueneHCID 1140—
생성물1,1,3-Trimethylindan-4-amineHCID 11217541—

반응 단계

Into a reaction vessel were charged 31.7 parts by weight of (3R)-1,1,3-trimethyl-4-aminoindane (optical purity of 67.0% ee) and 0.76 parts by weight of 5% palladium-carbon (E-type, manufactured by N. E. Chemcat Corporation), thereby obtaining a mixture. The reaction vessel was sealed and the gas in the reaction vessel was replaced with nitrogen. While the mixture was stirred, into the reaction vessel was charged hydrogen until the internal pressure of hydrogen in the reaction vessel reached 0.5 MPa, and the mixture was stirred at an internal temperature of 60° C. After 1 hour, the gas in the reaction vessel was replaced with nitrogen, and the mixture was stirred at an internal temperature of 145° C. and an internal pressure of 0.15 MPa for 14 hours, thereby obtaining a reaction mixture. The obtained reaction mixture was cooled and filtered. The obtained solid was washed with 45 parts by weight of toluene. The washing liquid recovered after washing and the filtrate obtained by filtration were combined to obtain a solution of 73.0 parts by weight of 1,1,3-trimethyl-4-aminoindane in toluene. The combined 1,1,3-trimethyl-4-aminoindane had an optical purity of 0.7% ee and a recovery rate of 97.7%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09284260B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-350778ab44784e048502f1de9decad6d
출처 메모uspto-grants-2016_03