Water → HCID 523368, compound

HRID 1384998Notes

Reaction equation

HRID 1384998 reaction equation
[OH:1][CH:2]1[CH2:7][CH2:6][O:5][C:3]1=[O:4].[CH3:8][Si:9](Cl)([CH3:11])[CH3:10].C(N(CC)CC)C.O>C1COCC1.CCOCC>[CH3:8][Si:9]([CH3:11])([CH3:10])[O:1][CH:2]1[CH2:7][CH2:6][O:5][C:3]1=[O:4]

Participants

7

Reactant 4

HCID 962WaterHCID 6397ChlorotrimethylsilaneHCID 8471TriethylamineHCID 545831alpha-Hydroxy-gamma-butyrolactone

Product 1

HCID 523368HCID 523368, compoundYield 90%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Procedure

A solution of 10.0 g (98 mmol) of α-hydroxy-γ-butyrolactone in 100 mL of anhydrous THF under argon was cooled to 0-5° C. with magnetic stirring. Addition of 14 mL (110 mmol) of trimethylsilyl chloride and 16 mL (115 mmol) of triethylamine immediately produced a white precipitate. The suspension was warmed to room temperature and stirred for 4 hours. The suspension was poured into a separatory funnel containing 100 mL of H2O and 500 mL of ether. The organic layer was washed with 50 mL of H2O, 50 mL of brine, dried (MgSO4) and concentrated. Purification (Kugelrohr distillation) provided 14.7 g (90% yield) of α-trimethylsilyloxy-γ-butyrolactone bp 80-100° C. (8 mm Hg).

Workup

  1. customimmediately produced a white precipitate
  2. additionThe suspension was poured into a separatory funnel
  3. washThe organic layer was washed with 50 mL of H2O, 50 mL of brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated
  6. distillationPurification (Kugelrohr distillation)

Sources & evidence

ORD record
ord-fe5a6ba13ab64d2193fd1f3129e68973
Source dataset
uspto-grants-2001_07
Patent number
US06262073B1

Reaction notes

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