HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vinyl hexanoate → (2R)-2-t-Butoxycarbonylamino-3-n-hexanoyloxy-2-methyl-1-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vinyl hexanoate | HCID 76451 | — |
| Reactant | tert-butyl N-(1,3-dihydroxy-2-methylpropan-2-yl)carbamate | HCID 11593669 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | (2R)-2-t-Butoxycarbonylamino-3-n-hexanoyloxy-2-methyl-1-propanol | HCID 11630856 | 85% |
Reaction Steps
To a suspension of 2-t-butoxycarbonylamino-2-methylpropane-1,3-diol (20.0 g, 97.4 mmol) in isopropyl ether (200 ml) were added successively vinyl hexanoate (16.3 ml, 0.10 mol) and lipase [Immobilized lipase from Pseudomonas sp., TOYOBO, 0.67 U/mg) (0.8 g) with stirring, and the resulting mixture was stirred at room temperature for 2 hours. After stirring, the reaction mixture was filtered and evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (10:1-2:1) as the eluent to afford the title compound (25.0 g, yield: 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07638551B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-9cb2bb11f42040a68a4be111671ae9a9 |
| Source note | uspto-grants-2009_12 |