HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyldiphenylchlorosilane → HCID 59268006, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | HCID 59267935 | HCID 59267935 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59268006 | HCID 59268006 | 116.1% |
Reaction Steps
To a solution of 0.41 g (0.96 mmol) of N-[3-(2-hydroxy-1,1-dimethyl-ethyl)-isoxazol-5-yl]-2-(4-methoxy-cyclohexylmethanesulfonyl)-2-methyl-propionamide in DCM (8 ml) are added imidazoles (0.07 g, 0.96 mmol), followed by tert-Butylchlorodiphenylsilane (0.26 g, 0.96 mmol). The reaction is stirred at room temperature for 20 h. The mixture is diluted with DCM (10 mL) and washed with saturated aqueous NH4Cl solution, brine, dried (MgSO4) and filtered. The filtrate is concentrated under reduced pressure to give 0.73 g of N-{3-[2-(tert-butyl-diphenyl-silanyloxy)-1,1-dimethyl-ethyl]-isoxazol-5-yl}-2-(4-methoxy-cyclohexylmethanesulfonyl)-2-methyl-propionamide. Yield: 100%, ES-MS: 655 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362039B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-e44d081b307a4479aa70d4a058d71491 |
| Source note | uspto-grants-2013_01 |