4-Cyanobenzaldehyde → tert-Butyl 1-(4-cyanobenzyl)azetidine-3-carboxylate

HRID 71221노트

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HRID 71221 반응식
C(O)(=O)C.[NH:5]1[CH2:8][CH:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:6]1.[C:16]([C:18]1[CH:25]=[CH:24][C:21]([CH:22]=O)=[CH:20][CH:19]=1)#[N:17].C([BH3-])#N.[Na+]>CO>[C:16]([C:18]1[CH:25]=[CH:24][C:21]([CH2:22][N:5]2[CH2:6][CH:7]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:8]2)=[CH:20][CH:19]=1)#[N:17]

참가 물질

5

반응물 3

HCID 660424-CyanobenzaldehydeHCID 5003444Sodium cyanoborohydrideHCID 66677484tert-Butyl azetidine-3-carboxylate acetate

생성물 1

HCID 58504367tert-Butyl 1-(4-cyanobenzyl)azetidine-3-carboxylate수율 89%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
0 °C

실험 절차

To a solution of tert-butyl azetidine-3-carboxylate acetic acid salt (92.0 g, 0.423 mol) in methanol (1.0 L) at room temperature was added 4-cyanobenzaldehyde (50.8 g, 0.381 mol). The reaction mixture was cooled to 0° C., and sodium cyanoborohydride (28.8 g, 0.458 mol) was added portion-wise. The reaction mixture was allowed to warm to room temperature and was stirred overnight. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with a 10% aqueous solution of sodium bicarbonate, extracted with ethyl acetate, washed with brine, and dried over anhydrous sodium sulfate. Concentration under reduced pressure followed by purification by flash silica gel column chromatography using a 20% mixture of ethyl acetate in petroleum ether afforded tert-butyl 1-(4-cyanobenzyl)azetidine-3-carboxylate (89%) (the desired product and alcohol impurity formed were not separated by column completely, and the mixture was taken for next step). LC/MS M+1=273.18. 1H-NMR (400 MHz, CDCl3) δ ppm 1.46 (s, 9H), 3.22-3.31 (m, 3H), 3.48-3.56 (m, 2H), 3.66 (s, 2H), 7.39 (d, J=8.28 Hz, 2H), and 7.60 (d, J=8.28 Hz, 2H).

후처리

  1. temperatureto warm to room temperature
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additionthe residue was diluted with a 10% aqueous solution of sodium bicarbonate
  4. extractionextracted with ethyl acetate
  5. washwashed with brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationConcentration under reduced pressure
  8. customfollowed by purification by flash silica gel column chromatography

출처 및 근거

ORD 기록
ord-9dccf2b77a524e0499fe009c59394402
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08822510B2

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