HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1,2,10-Decanetriol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Trimethylamine oxide | HCID 1145 | — |
| Reactant | 9-Decen-1-ol | HCID 25612 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1,2,10-Decanetriol | HCID 2735912 | — |
Reaction Steps
9-Decen-1-ol (25.0 g, 160 mmol) was dissolved in a solution made up of t-butanol (100 ml), acetone (90 ml) and water (10 ml). To this solution was added trimethylamine-N-oxide (26.6 g, 240 mmol) and 2 ml of a solution of osmium tetroxide (500 mg) in t-butanol (25 ml). The resulting solution was stirred 20 hours under nitrogen then 10% sodium bisulfite was added (50 ml). The mixture was concentrated, then taken up in trichloromethane and washed 2 times with water, dried with Na2SO4 and concentrated to give 1,2,10-decanetriol as an oil. This material was used without further purification in preparation of the corresponding acetonide (of formula 21).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05622712 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-31a1e74b8fe943d6bdee245abc523527 |
| Source note | uspto-grants-1997_04 |