Acetic Acid → N-(4-Bromobenzyl)-2,2-dimethoxyethanamine

HRID 522849노트

반응식

HRID 522849 반응식
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[CH3:10][O:11][CH:12]([O:15][CH3:16])[CH2:13][NH2:14].CC(O)=O.[BH4-].[Na+]>CO>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH:14][CH2:13][CH:12]([O:15][CH3:16])[O:11][CH3:10])=[CH:4][CH:3]=1

참가 물질

6

실험 절차

To an ice-cold solution of 4-bromo-benzaldehyde (10 g, 0.05 mol) and 2,2-dimethoxy-ethylamine (6.8 g, 0.06 mol) in MeOH (200 mL) was added AcOH (2 mL), and the reaction mixture was stirred at RT for 1 h. The reaction mixture was cooled to 0° C. and NaBH4 (6.2 g, 0.15 mol) was added portionwise. The reaction mixture was stirred at RT for 10 h. After completion, The resulting reaction mixture was concentrated under reduced pressure and 10% aqueous NaOH was added. The mixture was extracted with EtOAc, the organic layer separated, dried over Na2SO4, and concentrated under reduced pressure. Purification was done by column chromatography using 100-200 mesh silica gel eluting with 5-15% EtOAc in hexanes to afford N-(4-bromobenzyl)-2,2-dimethoxyethanamine (10 g, 67%) as a pale yellow liquid.

후처리

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. stirringThe reaction mixture was stirred at RT for 10 h
  3. customAfter completion, The resulting reaction mixture
  4. concentrationwas concentrated under reduced pressure and 10% aqueous NaOH
  5. additionwas added
  6. extractionThe mixture was extracted with EtOAc
  7. customthe organic layer separated
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated under reduced pressure
  10. customPurification

출처 및 근거

ORD 기록
ord-be8d3061f31b411a919d5233dcde361e
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09334269B2

반응 노트

불러오는 중…