HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Methyl 2-allyloctanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-Isopropyloxycarbonyl-N-(2-allyloctanoyl)-(R)-1-phenylethylamine | HCID 69502054 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-allyloctanoate | HCID 23117480 | — |
Reaction Steps
A solution of 0.374 g (1.0 mmol) of N-isopropyloxycarbonyl-N-(2-allyloctanoyl)-1-(R)-phenylethylamine ((1R,2S):(1R,2R)=77.6:22.4) in 5 ml of THF was cooled to 0° C. A solution of 11 mg (0.2 mmol) of NaOMe in methanol (0.04 g) was added, and the mixture was stirred for 7 hours. The reaction was terminated by addition of 1 ml of 1 N hydrochloric acid, and the product was extracted with ethyl acetate (30 ml×2). The extract was dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was quantitated by GC. Thus was obtained 0.163 g (82%, 55.0% ee) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07282605B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-56bcdcdd8cd44e3fbc51570e68e76f86 |
| Source note | uspto-grants-2007_10 |