HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzyloxy-5-(4-fluorophenoxy)-1-pentanol → 4(S)-Acetyloxynonanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzyloxy-5-(4-fluorophenoxy)-1-pentanol | HCID 21317584 | — |
| Reactant | 4(S)acetyloxy-1-nonanol | HCID 22800255 | — |
| Product | 4(S)-Acetyloxynonanal | HCID 22800256 | — |
Reaction Steps
This compound is prepared essentially by the method as described in Example 5, Step B-6, except that the 4-benzyloxy-5-(4-fluorophenoxy)pentanol is replaced by 4(S)acetyloxy-1-nonanol. This method provides the title compound as an essentially colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04102888 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-efddd44528a44f72abd052717d43ad44 |
| Source note | uspto-grants-1978_07 |