HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178454090, compound → HCID 178454089, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178454090 | HCID 178454090 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178454089 | HCID 178454089 | 100.4% |
Reaction Steps
To a solution of trans-(3-hydroxymethyl-cyclobutyl)-carbamic acid tert-butyl ester (Compound 4a) (0.2 g; 1.0 mmol) in anhydrous dichloromethane (8.0 mL) at 0° C. was added 1,1,1-tris(acetyloxy)-1,1-dihydro-1,2-benzodioxol-3-(1H)-one (0.84 g; 2.0 mmol). The reaction was allowed to stir at room temperature under nitrogen for 3 h, before partitioning the reaction mixture between dichloromethane and brine. The organic layer was washed with brine, dried over Na2SO4, filtered, and the solvent evaporated in vacuo to yield a crude oil. The crude oil was purified via flash column chromatography, eluting with 30% ethyl acetate in hexanes, to yield Compound 4b as a foam (0.2 g; 88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513271B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-ea9f10a0f8cb45728906560157d44137 |
| Source note | uspto-grants-2013_08 |