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Potassium Carbonate → 2-(4-(5-Bromo-2-chlorobenzyl)phenyl)ethanol

HRID 1175248
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반응식

HRID 1175248 반응식
C([O:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][C:14]2[CH:19]=[C:18]([Br:20])[CH:17]=[CH:16][C:15]=2[Cl:21])=[CH:9][CH:8]=1)(=O)C.C(=O)([O-])[O-].[K+].[K+]>CO.O>[Br:20][C:18]1[CH:17]=[CH:16][C:15]([Cl:21])=[C:14]([CH:19]=1)[CH2:13][C:10]1[CH:11]=[CH:12][C:7]([CH2:6][CH2:5][OH:4])=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11430Potassium CarbonateHCID 595577874-(5-Bromo-2-chlorobenzyl)phenethyl acetate

생성물 1

HCID 595577662-(4-(5-Bromo-2-chlorobenzyl)phenyl)ethanol수율 76%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

4-(5-bromo-2-chlorobenzyl)phenethyl acetate (intermediate BG) (400 mg, 1.09 mmol) and potassium carbonate (481 mg, 3.48 mmol) were stirred at room temperature in a mixture of 3 mL methyl alcohol and 0.5 mL water for 3 h. Solvents were evaporated and the residue taken up in 25 mL ether was washed with water (5 mL) and brine (20 mL), dried (Na2SO4), filtered and evaporated. Purification on silica gel using an ISCO column with 15:1 hexane:EtOAc gave intermediate BH (271 mg, yield 76%). 1H NMR (300 MHz, CDCl3): δ 7.27-7.07 (m, 7H), 4.02 (s, 2H), 3.84 (m, 2H), 2.86 (m, 3H); LC-ESI-MS (m/z): 325 (M+H).

후처리

  1. customSolvents were evaporated
  2. washwas washed with water (5 mL) and brine (20 mL)
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. customevaporated
  6. customPurification on silica gel using an ISCO column with 15:1 hexane
  7. customEtOAc gave intermediate BH (271 mg, yield 76%)

출처 및 근거

ORD 기록
ord-83abb2b59b79461fa8f7055de8cbc5af
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07838499B2

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