Hydrochloric Acid → 2-{[2-(2-Chlorophenyl)ethyl](methyl)amino}ethan-1-ol

HRID 2413109노트

반응식

HRID 2413109 반응식
B.[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][C:10]([N:12]([CH2:14][CH2:15][OH:16])[CH3:13])=O.Cl>O1CCCC1>[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][N:12]([CH3:13])[CH2:14][CH2:15][OH:16]

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6331BoraneHCID 133669682-chloro-N-(2-hydroxyethyl)-N-methylbenzeneacetamide

생성물 1

HCID 133669692-{[2-(2-Chlorophenyl)ethyl](methyl)amino}ethan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To 400 ml. of a 1 mol solution of borane in tetrahydrofuran was added dropwise a solution of 43 g. of the above amide in 350 ml. of tetrahydrofuran at a rate sufficient to maintain a gentle reflux. After addition was complete, the solution was refluxed for two hours, cooled in an ice bath and treated carefully with dilute hydrochloric acid to destroy excess borane. The majority of the solvent was removed under vacuum and the residue heated on a steam bath for one hour. The mixture was diluted with 300 ml. of water and extracted with ether. The aqueous layer was made basic with 40% sodium hydroxide and extracted with ether. The combined basic extracts were washed with water and saturated sodium chloride, dried and evaporated to give 2-[[2-(2-chlorophenyl)-ethyl]-methylamino]ethanol.

후처리

  1. additionAfter addition
  2. temperaturethe solution was refluxed for two hours
  3. temperaturecooled in an ice bath
  4. customto destroy excess borane
  5. customThe majority of the solvent was removed under vacuum
  6. temperaturethe residue heated on a steam bath for one hour
  7. additionThe mixture was diluted with 300 ml
  8. extractionof water and extracted with ether
  9. extractionextracted with ether
  10. washThe combined basic extracts were washed with water and saturated sodium chloride
  11. customdried
  12. customevaporated

출처 및 근거

ORD 기록
ord-8c0af4f70b2d42a5862a4a519edbc68e
출처 데이터셋
uspto-grants-1985_01
특허 번호
US04496558

반응 노트

불러오는 중…