Tetrahydrofuran → 5-(Tetrahydro-pyran-2-yloxy)-pent-2-yn-1-ol

HRID 2414646Notes

Reaction equation

HRID 2414646 reaction equation
[CH2:1]([O:5][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][O:7]1)[CH2:2][C:3]#[CH:4].C([Li])CCC.C1C[O:20][CH2:19]C1>>[O:7]1[CH2:8][CH2:9][CH2:10][CH2:11][CH:6]1[O:5][CH2:1][CH2:2][C:3]#[C:4][CH2:19][OH:20]

Participants

4

Conditions

Temperature
-23 °C

Procedure

To a solution of 8.0 mL (51 mmol) of 2-(3-butynyloxy)tetrahydro-2H-pyran in 150 mL of THF under nitrogen atmosphere at −23° C. was added dropwise a solution of 33 mL (53 mmol) of 1.6M butyllithium in hexanes, maintaining the temperature at −23° C. The resulting solution was stirred at 0° C. for 2 h, recooled to −23° C. and 2.4 g (76.5 mmol) of parafomaldehyde was added in several portions. The mixture was stirred at −23° C. for 1h and let warm to room temperature and stirred for 18 h. The reaction mixture was poured into a large excess of ice water and extracted with ether. The organics were washed with brine until neutral, dried over MgSO4, filtered and concentrated in vacuo. The residue was kugelrohr distilled to provide 7.26 g (77%) of 5-(tetrahydro-2H-pyran-2-yloxy)-2-pentyn-1-ol as a colorless liquid. EI Mass Spec: 185.1 (M+H)+

Workup

  1. customrecooled to −23° C.
  2. addition2.4 g (76.5 mmol) of parafomaldehyde was added in several portions
  3. temperaturelet warm to room temperature
  4. stirringstirred for 18 h
  5. extractionextracted with ether
  6. washThe organics were washed with brine until neutral,
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. distillationThe residue was kugelrohr distilled

Sources & evidence

ORD record
ord-7f8cce550f2f483dbb02f584a29675ce
Source dataset
uspto-grants-2004_11
Patent number
US06812227B2

Reaction notes

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