Carbon tetrabromide → methyl (1R,3S)-3-(bromomethyl)cyclopentane-1-carboxylate

HRID 537364노트

반응식

HRID 537364 반응식
O[CH2:2][C@H:3]1[CH2:7][CH2:6][C@@H:5]([C:8]([O:10][CH3:11])=[O:9])[CH2:4]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Br)(Br)(Br)[Br:32]>C(Cl)Cl>[Br:32][CH2:2][C@H:3]1[CH2:7][CH2:6][C@@H:5]([C:8]([O:10][CH3:11])=[O:9])[CH2:4]1

참가 물질

5

실험 절차

To a 0° C. solution of 99 (6.6 gm, 50 mmol, 1 equi.) in 60 mL of DCM was added triphenyl phosphine (60 mmol, 1.2 equi, 15.72 gm) followed by carbon tetrabromide (60 mmol, 1.2 equi. 19.86 gm). The reaction mixture was stirred overnight allowing the temperature to rise to room temperature. Reaction was concentrated to dryness and the residue was diluted with ether/DCM (1:1, 20 ml) and filtered through a pad of celite. The filtrate was concentrated to dryness and the residue was purified by silica gel chromatography with (5% to 20% EtOAc in hexanes) to provide 3.5 g of (1R,3S)-methyl 3-(bromomethyl)cyclopentanecarboxylate 100.

후처리

  1. customto rise to room temperature
  2. customReaction
  3. concentrationwas concentrated to dryness
  4. additionthe residue was diluted with ether/DCM (1:1, 20 ml)
  5. filtrationfiltered through a pad of celite
  6. concentrationThe filtrate was concentrated to dryness
  7. customthe residue was purified by silica gel chromatography with (5% to 20% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-0647b60b1b9a49d6853e74140732664d
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08859776B2

반응 노트

불러오는 중…