HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexene, 1-((trimethylsilyl)oxy)- → beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexene, 1-((trimethylsilyl)oxy)- | HCID 81161 | — |
| Reactant | (2R,3R)-(-)-2-Benzyloxy-1,3,4-butanetriol | HCID 10867592 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol | HCID 53702433 | 96,624.102% |
Reaction Steps
4.34 g (0.02 mol) of (2R,3R)-2-benzyloxybutane-1,3,4-triol were suspended in a mixture of 3.4 g (0.02 mmol) of 1-cyclohexenyloxytrimethylsilane and 40 ml of diethyl ether. Two drops of concentrated hydrochloric acid were added and the mixture was stirred at room temperature for 30 minutes. The mixture was then evaporated to give 5.65 g of β(R) -benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol in the form of a colourless viscous oil; MS: m/e 292 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516913 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-bd3fcfa9c2394d11a2c7feea445d9800 |
| Source note | uspto-grants-1996_05 |