HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,5-Dibromopentane → HCID 21407936, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl bromo(4-chlorophenoxy)acetate | HCID 12376161 | — |
| Reactant | HCID 21407938 | HCID 21407938 | — |
| Reactant | HCID 57241026 | HCID 57241026 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 21407936 | HCID 21407936 | — |
Reaction Steps
2.3 g. of 1,5-dibromopentane, 3.2 g. of (4-chlorophenoxy)-(4-aminophenoxy)-acetic acid ethyl ester [obtainable by reacting Na-4-nitrophenolate with α-bromo-α-(4-chlorophenoxy)-acetic acid ethyl ester to obain the ethyl ester of (4-chlorophenoxy)-(4-nitrophenoxy)-acetic acid and subsequent hydrogenation], and 1.4 g. of K2CO3 are refluxed for 12 hours in 40 ml. of n-butanol. As an intermediate compound, the ethyl ester of (4-chlorophenoxy)-[4-(5-bromopentylamino)-phenoxy]-acetic acid is produced. After working up the mixture as usual, (4-chlorohenoxy)-(4-piperidinophenoxy)-acetic acid ethyl ester is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04051170 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-60bee018ddd545439c9c7c075783bad3 |
| Source note | uspto-grants-1977_09 |