HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (+)-trans-1-t-Butyldimethylsilyloxymethyl-4-oxo-2-phenylcyclopentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | (+-)-trans-1-t-Butyldimethylsilyloxymethyl-4-methylene-2-phenylcyclopentane | HCID 18686191 | — |
| Product | (+)-trans-1-t-Butyldimethylsilyloxymethyl-4-oxo-2-phenylcyclopentane | HCID 18686192 | — |
Reaction Steps
Into a solution of (+−)-trans-1-t-butyldimethylsilyloxymethyl-4-methylene-2-phenylcyclopentane from Step B1 (2.2 g, 7.3 mmol) in methanol (100 mL) cooled in a dry ice/acetone bath was bubbled ozone until the blue color persisted. The excess ozone was removed with a stream of nitrogen and then dimethylsulfide (5 mL) was added. After 10 min, the bath was removed and the reaction was allowed to warm to rt over 2 h. The volatiles were removed in vacuo and the residue was purified by FC (15-30% ethyl acetate in hexanes) to give the title compound (1.9 g) which was the same as in Method A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506777B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-752c839283fa4b6e8bfa4fcfd035f5c8 |
| Source note | uspto-grants-2003_01 |