HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-acetoxynonane → 7-[N-(4-hydroxy-2-noneneyl)acetamido]heptanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-acetoxynonane | HCID 13104716 | — |
| Reactant | ethyl 7-[N-(4-acetoxy-(E)-2-nonenyl)acetamido]-heptanoate | HCID 21503934 | — |
| Reactant | 1-Bromo-4-acetoxy-2-nonene | HCID 54048569 | — |
| Product | 7-[N-(4-hydroxy-2-noneneyl)acetamido]heptanoic acid | HCID 54446276 | — |
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-bromo-4-acetoxy-2-nonene (Example H). The product of Step B is ethyl 7-[N-(4-acetoxy-(E)-2-nonenyl)acetamido]-heptanoate. The subsequent step yields 7-[N-(4-hydroxy-2-noneneyl)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-90be85c0ec5e450faa57901a0d4788f1 |
| Source note | uspto-grants-1976_10 |