HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → Cetirizine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2-Chloroethoxy)acetic acid | HCID 10920584 | — |
| Reactant | 2-(2-Chloroethoxy)acetamide | HCID 11018931 | — |
| Reactant | 2-(2-Chloroethoxy)acetonitrile | HCID 14835913 | — |
| Reactant | 2-Chloroethoxy acetate | HCID 18435677 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Cetirizine | HCID 2678 | — |
Reaction Steps
The compound (I) may be further treated with a 2-chloroethoxy acetic acid derivative such as 2-chloroethoxy acetamide or 2-chloroethoxy acetate or 2-chloroethoxy acetonitrile in the presence of a base such as sodium carbonate or potassium carbonate, and a solvent such as toluene or xylene to obtain the corresponding [2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]acetic acid derivative which on hydrolysis, for example, using sodium hydroxide gives levocetirizine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08350031B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-0709d4e8829142cd93bbdf1360d5fbd2 |
| Source note | uspto-grants-2013_01 |