HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-Methoxy-2-oxoethyl 2-hydroxy-2-methylbutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tert-Butylbenzene | HCID 7366 | — |
| Reactant | Methyl Glycolate | HCID 66774 | — |
| Reactant | 2-Chloroethyl 2-hydroxy-2-methylbutyrate | HCID 18953220 | — |
| Product | 2-Methoxy-2-oxoethyl 2-hydroxy-2-methylbutyrate | HCID 54293197 | — |
Reaction Steps
A 6 mL aliquot of an ethyl ether solution containing 0.25M 2-chloroethyl 2-hydroxy-2-methyl-butyrate, 0.25M methyl glycolate, and 1.0% tert-butylbenzene was added to 0.4 g Lipase P30. After mixing for 7 d at room temperature, the conversion of 2-chloroethyl 2-hydroxy-2-methylbutyrate to the title compound was estimated (by GC, Method A) to be approximately 10%. The GC peak assigned to the title compound was confirmed by HRMS: calcd for C7H10O5Tms (M-CH3) 247.1001, obsd 247. 0998. In identical reactions substituting Lipase MAP10, Lipase G, Lipase AK, or porcine pancreatic lipase for Lipase P30, the relative values for conversions at 7 d (Lipase P30=100) were 73, 21, 16, and 0, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371001 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-ffd42fab891b4885b578bb75355ec20b |
| Source note | uspto-grants-1994_12 |