Dimethylamine → 1-(4-ethynylphenyl)-N,N-dimethylmethanamine

HRID 447340

반응식

HRID 447340 반응식
[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1)#[CH:2].[CH3:11][NH:12][CH3:13].[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>C(O)(=O)C.ClCCCl>[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH2:7][N:12]([CH3:13])[CH3:11])=[CH:5][CH:4]=1)#[CH:2]

참가 물질

6

반응물 3

HCID 674DimethylamineHCID 27716454-EthynylbenzaldehydeHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 866588291-(4-ethynylphenyl)-N,N-dimethylmethanamine수율 92%

시약·촉매·용매 2

HCID 176Acetic Acid촉매HCID 111,2-Dichloroethane용매

실험 절차

Glacial acetic acid (3 drops) was added to a mixture of 4-ethynylbenzaldehyde (250.7 mg, 1.93 mmol), dimethylamine (2M in THF, 1.5 mL, 3.0 mmol) and NaBH(OAc)3 (617 mg, 2.91 mmol) in DCE (6.5 mL). The resulting mixture was stirred for 2.5 h at rt. The reaction was quenched with saturated aqueous NaHCO3 (−40 mL). The product was extracted into CH2Cl2 (100 mL, then 2×50 mL), and the combined organic layer was washed with brine (25 mL), dried (Na2SO4) and evaporated in vacuo. Purification on Biotage Isolera (silica, 0-3% 2M NH3-methanol/CH2Cl2) gave 1-(4-ethynylphenyl)-N,N-dimethylmethanamine (280.1 mg, 92%). 1H NMR (400 MHz, CDCl3) δ 7.46 (d, J=8 Hz, 2H), 7.28 (d, J=8 Hz, 2H), 3.42 (s, 2H), 3.07 (s, 1H), 2.24 (s, 6H).

후처리

  1. customThe reaction was quenched with saturated aqueous NaHCO3 (−40 mL)
  2. extractionThe product was extracted into CH2Cl2 (100 mL
  3. wash2×50 mL), and the combined organic layer was washed with brine (25 mL)
  4. dry with materialdried (Na2SO4)
  5. customevaporated in vacuo
  6. customPurification on Biotage Isolera (silica, 0-3% 2M NH3-methanol/CH2Cl2)

출처 및 근거

ORD 기록
ord-3756c77c2cee4e638181519a58b0f3b6
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08481533B2

연결된 노트

불러오는 중…