HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (1-Allyl-3-methylcyclobutoxy)(tert-butyl)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Reactant | 1-Allyl-3-methylcyclobutanol | HCID 67305235 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-Allyl-3-methylcyclobutoxy)(tert-butyl)dimethylsilane | HCID 67304682 | — |
Reaction Steps
1-Allyl-3-methylcyclobutanol (2.25000 g, 17.8 mmol) (the 4:1 mixture of cis/trans-isomers) was dissolved in 50 ml of CH2Cl2 and DIEA (5.59 ml, 32.1 mmol) and tert-butyldimethylsilyl triflate (5.73 ml, 25.0 mmol) were added. The mixture was stirred for 2 h and hydrolyzed with water, extracted with 200 ml Et2O (3× each), dried over MgSO4 and evaporated. Glass col. chrom. (10-30% EtOAc in Hex.) provided (1-allyl-3-methylcyclobutoxy)(tert-butyl)dimethylsilane as a yellow oil. Mixture of cis/trans at the cyclobutylring (4:1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07973047B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-f099db0c0c57416eb2ddce88edccb8e2 |
| Source note | uspto-grants-2011_07 |