HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 7-Acetoxy-2-(5-methoxyhept-1-y)bicyclo[3.3.0]octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Octahydro-4-(5-methoxyheptyl)-2-pentalenol | HCID 15053012 | — |
| Product | 7-Acetoxy-2-(5-methoxyhept-1-y)bicyclo[3.3.0]octane | HCID 15053046 | — |
Reaction Steps
The procedure followed is the same as that described in Example 24 substituting 2-(5-methoxyhept-1-yl)bicyclo[3.3.0]-7octanol {octahydro-4-(5-methoxyheptyl)-2-pentalenol} (1.0 g, 4.0 mmoles), and glacial acetic acid (7 ml). The product is kugelrohred under reduced pressure leaving a clear, colorless oil (0.7 g, 2.5 mmoles).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04689345 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-8925cec102084632920e4fddf72535c1 |
| Source note | uspto-grants-1987_08 |