HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 523368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | alpha-Hydroxy-gamma-butyrolactone | HCID 545831 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 523368 | HCID 523368 | 90% |
Reaction Steps
A solution of 10 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06136832 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-d87697cfd120474489fc39fdaf89a575 |
| Source note | uspto-grants-2000_10 |