Hydrochloric Acid → N-[8-(naphthalen-2-ylmethyl)-8-azabicyclo[3.2.1]oct-3-yl]amine

HRID 29928

반응식

HRID 29928 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][N:12]1[CH:17]2[CH2:18][CH2:19][CH:13]1[CH2:14][CH:15]([NH:20]C(=O)C)[CH2:16]2.Cl.[OH-].[Na+]>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][N:12]1[CH:13]2[CH2:19][CH2:18][CH:17]1[CH2:16][CH:15]([NH2:20])[CH2:14]2

참가 물질

4

실험 절차

4 g (12.9 mmol) of N-[8-(naphthalen-2-ylmethyl)-8-azabicyclo[3.2.1]oct-3-yl]acetamide are poured into 13 mL of 5N hydrochloric acid. The mixture is refluxed for 4 hours and then cooled in an ice bath, basified with 35% sodium hydroxide and extracted three times with ethyl acetate. The combined extracts are washed with water and with brine, dried over anhydrous sodium sulfate and then evaporated under reduced pressure. 3.2 g of oily product are obtained (94% yield).

후처리

  1. temperatureThe mixture is refluxed for 4 hours
  2. temperaturecooled in an ice bath
  3. extractionextracted three times with ethyl acetate
  4. washThe combined extracts are washed with water and with brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-3bcc88a025b542d58ecc20193d1d1b3c
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07423030B2

연결된 노트

불러오는 중…