Hydrochloric Acid → 4-(iodomethyl)tetrahydro-2H-pyran-4-ol

HRID 869653Notes

Reaction equation

HRID 869653 reaction equation
[Cl-].[CH3:2][S+](C)(C)=O.[OH-:7].[Na+].O1[CH2:14][CH2:13][C:12](=[O:15])[CH2:11][CH2:10]1.[I-:16].[Na+].Cl>O1CCCC1.C(OCC)(=O)C>[I:16][CH2:2][C:12]1([OH:15])[CH2:13][CH2:14][O:7][CH2:10][CH2:11]1

Participants

8

Conditions

Temperature
50 °C

Procedure

A mixture of trimethylsulfoxonium chloride (3.08 g, 23.73 mmol) and 2 N aq. sodium hydroxide (11.33 mL, 22.65 mmol) in tetrahydrofuran (13 mL) was heated at 50° C. for 1 h. 2.16 g (21.57 mmol) of tetrahydro-4H-pyran-4-one was added to the mixture and the mixture was stirred at 50° C. for 30 min. After cooling to room temperature, 3.56 g (23.73 mmol) of sodium iodide and 2 N hydrochloric acid (10.8 mL, 21.57 mmol) were added to the mixture. After being stirred at room temperature for 19 h, ethyl acetate was added to the mixture. The mixture was extracted with ethyl acetate three times and the extracts were combined. The extracts were dried over sodium sulfate and concentrated in vacuo to afford a beige solid. The residual solid was recrystallized from acetonitrile to afford 3.13 g (55%) of the title compound.

Workup

  1. temperatureAfter cooling to room temperature
  2. stirringAfter being stirred at room temperature for 19 h
  3. extractionThe mixture was extracted with ethyl acetate three times
  4. dry with materialThe extracts were dried over sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customto afford a beige solid
  7. customThe residual solid was recrystallized from acetonitrile

Sources & evidence

ORD record
ord-2e5855b1ef5245b7933775267b41d8b2
Source dataset
uspto-grants-2015_03
Patent number
US08969383B2

Reaction notes

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