HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylbenzene → 2-(1-Methylethoxy)-2-oxoethyl 2-hydroxy-3-phenylpropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylbenzene | HCID 7366 | — |
| Reactant | Isopropyl hydroxyacetate | HCID 69338 | — |
| Reactant | 2-Chloroethyl 2-hydroxy-3-phenylpropionate | HCID 18953230 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(1-Methylethoxy)-2-oxoethyl 2-hydroxy-3-phenylpropionate | HCID 54030227 | — |
Reaction Steps
A 6 mL aliquot of an ethyl ether solution containing 0.25M 2-chloroethyl 2-hydroxy-3-phenylpropionate, 0.25M isopropyl glycolate, and 1.0% tert-butylbenzene was added to 0.43 g Lipase AK. After mixing for 2 d at room temperature, the conversion of 2-chloroethyl 2-hydroxy-3-phenylpropionate to the title compound was estimated (by GC, Method B) to be approximately 28%. The GC peak assigned to the title compound was confirmed by HRMS: calcd for C13H14O5Tms (M-CH3) 323. 1314, obsd 323. 1290. In identical reactions substituting Lipase P30, Lipase G, Lipase MAP10, porcine pancreatic lipase, Lipase AP12 or Protease M for Lipase AK, the relative values for conversions at 2 d (Lipase AK=100) were 88, 85, 76, 51, 7, and 7%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371001 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-5b94bdcc06c74f06a02a0d03821608e0 |
| Source note | uspto-grants-1994_12 |