1,3-Dibromobenzene → 4-(3-Bromophenyl)-tetrahydro-2H-pyran-4-ol

HRID 2060761노트

반응식

HRID 2060761 반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Br:8])[CH:3]=1.C([Li])CCC.CCCCCC.[O:20]1[CH:25]=[CH:24][C:23](=[O:26])[CH:22]=[CH:21]1>C1COCC1>[Br:8][C:4]1[CH:3]=[C:2]([C:23]2([OH:26])[CH2:24][CH2:25][O:20][CH2:21][CH2:22]2)[CH:7]=[CH:6][CH:5]=1

참가 물질

6

반응물 4

HCID 79271,3-DibromobenzeneHCID 79684H-pyran-4-oneHCID 8058HexaneHCID 178418339Butyllithium

생성물 1

HCID 189962824-(3-Bromophenyl)-tetrahydro-2H-pyran-4-ol수율 76%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred −78° C. solution of 1,3-dibromobenzene (19.71 g, 81.05 mmol) in THF (150 mL) is added 1.6 M butyl lithium in hexane (50.66 mL, 81.05 mmol) and the reaction is stirred 10 minutes. 4H-Pyran-4-one, tetrahydro- (5.41 g, 54.04 mmol) is added dropwise and the reaction is stirred at −78° C. for 2 h. The reaction is quenched by addition of saturated aqueous ammonium chloride (25 mL) and is then diluted with minimal water and extracted with EtOAc. The organic layer is dried over Na2SO4 and the solvent is removed under reduced pressure to afford a residue that is purified by silica gel chromatography eluting with a linear gradient of 5% to 100% EtOAc in hexanes to give the title compound (11.18 g, 76%). GC-MS (m/e): (79Br/81Br) 256, 258 (M−1).

후처리

  1. stirringthe reaction is stirred at −78° C. for 2 h
  2. customThe reaction is quenched by addition of saturated aqueous ammonium chloride (25 mL)
  3. additionis then diluted with minimal water
  4. extractionextracted with EtOAc
  5. dry with materialThe organic layer is dried over Na2SO4
  6. customthe solvent is removed under reduced pressure
  7. customto afford a residue that
  8. customis purified by silica gel chromatography
  9. washeluting with a linear gradient of 5% to 100% EtOAc in hexanes

출처 및 근거

ORD 기록
ord-ccddfd7d55b64b2e9e7c17975147f7ed
출처 데이터셋
uspto-grants-2012_10
특허 번호
US08278441B2

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