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Hydrogen Bromide → HCID 54525055, 화합물

HRID 1169189
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HRID 1169189 반응식
[CH:1]1([CH:6]2[CH2:10][O:9][C:8](=O)[CH2:7]2)[CH2:5][CH2:4][CH2:3][CH2:2]1.[BrH:12].[CH3:13][CH2:14][OH:15]>O>[CH2:14]([O:15][C:8](=[O:9])[CH2:7][CH:6]([CH2:10][Br:12])[CH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 260Hydrogen BromideHCID 702EthanolHCID 12664736HCID 12664736, 화합물

생성물 1

HCID 54525055HCID 54525055, 화합물수율 85%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Preparation of 3-bromomethyl-3-cyclopentyl-propionic acid ethyl ester—A solution of 4-cyclopentyl-dihydro-furan-2-one (4.4 g, 28.5 mmol) in 100 mL of EtOH is saturated with HBr at 0° C. The mixture is warmed to room temperature overnight. It is diluted with 200 mL of H2O and extracted with Et2O (3,100 mL). The combined extracts are washed with brine (2.50 mL) and dried over MgSO4. Evaporation of Et2O gives 6.4 g (85% yield) of 3-bromomethyl-3-cyclopentyl-propionic acid ethyl ester as a clear oil. NMR (1H, 400 MHz, CDCl3) δ1.1 (2H, m); 1.2 (3H, t); 1.5 (4H, m); 1.8 (3H, m); 1.9 (1H, m); 2.4 (2H, dd); 3.5 (2H, dd); 4.1 (2H,q).

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후처리

  1. extractionextracted with Et2O (3,100 mL)
  2. washThe combined extracts are washed with brine (2.50 mL)
  3. dry with materialdried over MgSO4
  4. customEvaporation of Et2O

출처 및 근거

ORD 기록
ord-f1e7977ea59d4733b8e9bc2ca0d4cf0f
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06627771B1

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