HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → tert-butyl (5R)-1-oxaspiro[2.5]octan-5-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (3-Oxo-cyclohexyl)-carbamic acid tert-butyl ester | HCID 44228975 | — |
| Product | tert-butyl (5R)-1-oxaspiro[2.5]octan-5-ylcarbamate | HCID 86698241 | — |
Reaction Steps
To a solution of Me3SOI (56.2 mmol) in DMSO (80 ml) was added NaH (51.5 mmol) and stirred at room temperature for 2 h until the solution become clear. The resulting solution was added tert-butyl 3-oxocyclohexylcarbamate (23.4 mmol) and stirred at rt overnight. The reaction was quenched with water and extracted with hexane. The extracts were combined and dried using anhydrous sodium sulfate. The product was purified using Biotage. The final products, isomer 1 and isomer 2, were well separated on silicon column with 15%-20% ethyl acetate in hexane. Each single diastereomer was used for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09351965B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-9e2d1b2685c74d4189e29bf6c505545e |
| Source note | uspto-grants-2016_05 |