Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | HCID 18730405 | HCID 18730405 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 14572861 | HCID 14572861 | — |
Reaction Steps
A solution of the product of Example 31A (1.1 gm, 5.9 mmol) was dissolved in CH2Cl2/MeOH 10:1 (15 mL) and cooled to −78° C. To the solution was bubbled O3 over 20 minutes. The reaction solution was purged with N2 for a further 10 minutes and dimethyl sulfide (DMS) (3.6 gm, 59 mmol) was added and the reaction warmed to ambient temperature and stirred for a further 2 hours. The solvent was evaporated in vacuo and product purified by flash column chromatography (hexane/EtOAc 100:0 to 70:30) to collect Example 31B as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | USRE041135E1 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-d7bf085c97e1470c9f22af813b1d56d0 |
|---|
| Source note | uspto-grants-2010_02 |
|---|