HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propylene Oxide → HCID 86720727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Butyl cyclopropanesulfonate | HCID 10464888 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86720727 | HCID 86720727 | — |
Reaction Steps
A solution of butyl cyclopropanesulfonate 2 (1.2 g, 6.7 mmol) in THF (24 mL) was cooled to −78° C. and n-butyllithium (1.6M in n-hexane, 5.0 mL, 8.1 mmol) was added within 5 min. The mixture was stirred for 30 min and epoxypropane derivative 1 or 8 (8.1 mmol) was added followed by addition of boron trifluoride diethyl etherate (0.84 mL, 6.7 mmol). The solution was stirred for 1 h at −78° C., the cooling bath was removed and stirring was continued for 2 additional hours. For aqueous work-up diluted hydrochloric acid (10%, 0.8 mL), water (10 mL) and ethyl acetate (20 mL) were added. The organic layer was is concentrated at 40° C. to afford the corresponding butyl 1-[2-hydroxypropyl]cyclopropanesulfonate 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328066B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-e0e139131b4f49a5a01878abc898c9f1 |
| Source note | uspto-grants-2016_05 |