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-methyloxycarbonyl-N-(2-allyloctanoyl)-1-(R)-phenylethylamine | HCID 69502051 | — |
| Product | Methyl 2-allyloctanoate | HCID 23117480 | 55% |
Reaction Steps
A solution of 0.345 g (1.0 mmol) of N-methyloxycarbonyl-N-(2-allyloctanoyl)-1-(R)-phenylethylamine in 5 ml of THF was cooled to 0° C., 0.386 g (2.0 mmol) of NaOMe (28% solution in methanol) was added, and the mixture was stirred for 22 hours. The reaction was terminated by addition of 2 ml of 1 N hydrochloric acid, and the product was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, the solvent was distilled off, and the residue was quantitated by GC. Thus was obtained 0.109 g (55%) 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-33279d8c9f2c4023a10c45151be4af4a |
| Source note | uspto-grants-2007_10 |