HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyldiphenylchlorosilane → HCID 10718325, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | .beta.-D-Galactopyranoside, methyl 1-thio- | HCID 10036019 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10718325 | HCID 10718325 | 81% |
Reaction Steps
A mixture of methyl 1-thio-β-D-galactopyranoside (25) 5 g, 28 mmol), chloro t-butyldiphenylsilane (5.85 g, 21 mmol) and DMAP (2.63 g, 21 mmol) in dry 1,2-dichloroethane (130 mL) was left to stir at reflux for 2.5 h. The reaction mixture was cooled to room temperature, diluted with dichloromethane (200 mL) and washed with saturated sodium chloride solution (2×250 mL). The organic phase was dried over MgSO4 and subsequently evaporated to dryness to give methyl 6-O-(t-butyldiphenylsilyl)-1-thio-β-D-galactopyranoside (26) (7.5 g, 81%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06953850B1 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-ad8ef44fda744f829c021ed2da81fc07 |
| Source note | uspto-grants-2005_10 |