홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

(+)-1-(1-Naphthyl)ethylamine → 1-(1-Naphthyl)ethylamine

HRID 1915195
노트
인쇄 미리보기

반응식

HRID 1915195 반응식
[C:1]1([C@H:11]([NH2:13])[CH3:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.FC(F)(F)C1C=C(C=CC=O)C=CC=1>CO>[C:1]1([CH:11]([NH2:13])[CH3:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2724264(+)-1-(1-Naphthyl)ethylamineHCID 534010893-[3-(Trifluoromethyl)phenyl]-2-propenal

생성물 1

HCID 980891-(1-Naphthyl)ethylamine

시약·촉매·용매 1

HCID 887Methanol용매2회

반응 조건

온도
25 °C

실험 절차

23.1 Kg of (R)-(+)-1-(1-naphthyl)ethylamine, 150.2 Kg of methyl alcohol, 27.7 Kg of 3-[3-(trifluoromethyl)phenyl]propenaldehyde were loaded in a reactor. The mass was stirred at a temperature of 20-30° C. for a few hours, thereby obtaining the non isolated intermediate (R)—N-[3-[3-(trifluoromethyl)phenyl]-2-propenylimino-N-[1-(1-naphthyl)ethylamine (IV) in a methanol solution. The intermediate was reduced by pouring a solution of 3.9 Kg of sodium borohydride dissolved in 46.2 Kg of methanol and 0.6 of 30% sodium hydrate in the mass. The mass was stirred at a temperature of 0-20° C. until the Schiff base was reduced. 4.9 Kg of 80% acetic acid were then poured and methanol was distilled. 207.9 Kg of toluol and 138.6 Kg of water were added to the residue and the mass was stirred, separated and then the aqueous phase was discarded.

출처 및 근거

ORD 기록
ord-d0a7ceb208924775a94335aa4f747bb2
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08614354B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차출처 및 근거반응 노트