HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(4-Phenylbutoxy)hept-6-en-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-(4-Phenylbutoxy)propionaldehyde | HCID 86658307 | — |
| Reactant | HCID 178418797 | HCID 178418797 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Phenylbutoxy)hept-6-en-3-ol | HCID 67244432 | 58.7% |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
A solution of Intermediate 13 (0.55 g, 2.66 mmol) in THF (5 mL) was cooled to −30° C. To this solution a 0.5 M solution of 3-butenylmagnesium bromide (5.8 mL, 2.92 mmol) in THF was added, and the resulting mixture was stirred 2 hours at −30° C. The reaction was allowed to reach room temperature; acetic acid (0.1 mL) was added and concentrated. Purification by column chromatography with silica gel and methylene chloride/acetone (20:1) as eluent afforded the title compound (410 mg, 54%) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420669B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-575ebb162e2c476aaf925a0987c21818 |
| Source note | uspto-grants-2013_04 |