HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 3-Dodecyl-5-isoxazole acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 3-Dodecyl-5-methylisoxazole | HCID 10491386 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Dodecyl-5-isoxazole acetic acid | HCID 10494110 | — |
Reaction Conditions
| Temperature | -75 °C |
|---|
Reaction Steps
To a cold (-75° C.), stirred suspension of 3-dodecyl-5-methylisoxazole (3.40 g, 0.0135 mol) in dry tetrahydrofuran (900 mL) was added in one portion a 1.6M solution (8.5 mL, 0.014 mol) of n-butyl lithium in hexanes, and the mixture was stirred for 1.5 hours. The mixture was poured onto freshly crushed dry ice and allowed to warm overnight. The mixture was rotoevaporated, and the residue was partitioned between petroleum ether and 0.5M NaOH. The aqueous layer was washed (petroleum ether), acidified with concentrated hydrochloric acid to pH ~1-2, and extracted (CHCl3). The extract was dried (MgSO4) and rotoevaporated to a waxy solid. The solid was recrystallized from toluene to give a white solid; yield 0.65 g (16%); mp 79°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441975 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-892c4a67311f48e0ae1268c84020bc41 |
| Source note | uspto-grants-1995_08 |