HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-acetoxynonane → 7-[N-(4(R)-hydroxy-2-nonynyl)acetamido]heptanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-acetoxynonane | HCID 13104716 | — |
| Reactant | 1-Chloro-4-acetoxy-5,5-dimethylnonane | HCID 20386107 | — |
| Reactant | ethyl 7-[N-(4-acetoxy-5,5-dimethylnonyl)acetamido]heptanoate | HCID 21503963 | — |
| Product | 7-[N-(4(R)-hydroxy-2-nonynyl)acetamido]heptanoic acid | HCID 22793820 | — |
Reaction Steps
The synthesis of this compound is carried out as described in Example 2 except that, in Step B, the 1-chloro-4-acetoxynonane is replaced by an equimolar amount of 1-chloro-4-acetoxy-5,5-dimethylnonane (Example G, Step 3). The product in Step B is ethyl 7-[N-(4-acetoxy-5,5-dimethylnonyl)acetamido]heptanoate. The subsequent step yields 7-[N-(4-hydroxy-5,5-dimethylnonyl)acetamido]-heptanoic acid (C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987091 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-1d48e0ae950247b084e1a775ec8a1bb6 |
| Source note | uspto-grants-1976_10 |