p-Toluenesulfonic acid → 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol

HRID 1943082노트

반응식

HRID 1943082 반응식
[O:1]1[CH:6]=[CH:5][CH2:4][CH2:3][C:2]1=[O:7].[CH2:8](O)[C:9]#[C:10][CH2:11][OH:12].CC1C=CC(S(O)(=O)=O)=CC=1.C(=O)(O)[O-].[Na+].C(=O)([O-])[O-].[K+].[K+]>ClCCl.O>[O:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH:2]1[O:7][CH2:8][C:9]#[C:10][CH2:11][OH:12]

참가 물질

8

실험 절차

3,4-Dihydro-2H-pyron (18.3 mL, 0.196 mol) in dichloromethane (30 mL) was added dropwise over 30 minutes to a stirred solution of 2-butyne-1,4-di-ol (16.832 g, 0.194 mol) and p-TsOH (2.236 g, 11.58 mmol) in DCM (250 mL) at 0° C. After addition, the mixture was stirred at room temperature for 4 hours. Sodium bicarbonate (858 mg) was added. The mixture was stirred for another hour. Water (10 mL) was added, followed by addition of saturated aqueous potassium carbonate (150 mL). The organic phase was separated and washed with brine (200 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure (temperature below 25° C.). The residue was separated by flash column chromatography on silica gel using 5-25% EtOAc/hexane to afford 12.88 g of product (yield: 39%), along with 12.05 g of di-protected side product. 1H-NMR (CDCl3): δ 4.78 (t, J=3.0-3.3 Hz, 1 H), 4.37-4.21 (m, 4 H), 3.86-3.78 (m, 1 H), 3.55-3.50 (m, 1 H), 1.83-1.64 (m, 6 H).

후처리

  1. additionAfter addition
  2. stirringThe mixture was stirred for another hour
  3. customThe organic phase was separated
  4. washwashed with brine (200 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure (temperature below 25° C.)
  7. customThe residue was separated by flash column chromatography on silica gel using 5-25% EtOAc/hexane

출처 및 근거

ORD 기록
ord-9d8a6ab6eea34d91a8ccc62b0bb99d80
출처 데이터셋
uspto-grants-2013_03
특허 번호
US08389759B2

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