HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 7-bromoheptanoate → Ethyl 7-{acetyl[4-(acetyloxy)nonyl]amino}heptanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 7-bromoheptanoate | HCID 122490 | — |
| Reactant | 1-Chloro-4-acetoxynonane | HCID 13104716 | — |
| Reactant | HCID 21503952 | HCID 21503952 | — |
| Reactant | Ethyl 7-acetamidoheptanoate | HCID 21503972 | — |
| Product | Ethyl 7-{acetyl[4-(acetyloxy)nonyl]amino}heptanoate | HCID 21503950 | — |
Reaction Steps
The preparation of this compound is accomplished by essentially the same method as described in Example 1, Step A, except that the N-[4-(2-tetrahydropyranyloxy)nonyl]-acetamide of Example 1, Step A is replaced by an equimolar quantity of ethyl 7-acetamidoheptanoate and the ethyl 7-bromoheptanoate is replaced by an equimolar quantity of 1-chloro-4-acetoxynonane (Example A, Step 4). Purification of the product by column chromatography on silica gel gives ethyl 7-[N-(4-acetoxynonyl)acetamido]heptanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987091 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-ed8f2477a0d2458e8571e85f5f202046 |
| Source note | uspto-grants-1976_10 |