HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloro-4-nitrobenzene → Methyl 2-[4-(2-chloro-4-nitrophenoxy)phenoxy]propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloro-4-nitrobenzene | HCID 7443 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Propanoic acid, 2-(4-hydroxyphenoxy)-, methyl ester | HCID 366926 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Methyl 2-[4-(2-chloro-4-nitrophenoxy)phenoxy]propanoate | HCID 12883848 | — |
Reaction Steps
6.5 g of pulverised potassium hydroxide and 20 g of methyl 4-hydroxy-α-phenoxypropionate in 250 ml of dry dimethyl sulphoxide are charged at 0° C. into a three-necked flask. With stirring, and at a temperature between 0° and 5° C., 19.5 g of 3,4-dichloro-nitrobenzene are added by small amounts and stirring is continued for 12 hours at room temperature. Thereafter the reaction mixture is poured into ice-water and extracted with ethyl acetate. The extract is dried over sodium sulphate and the solvent distilled off to yield an oily product which is then subjected to high vacuum distillation. The resultant substance, viz. methyl 4-(2'-chloro-4'-nitrophenoxy)-α-phenoxypropionate (yield 27 g), boils at 194° C./0.01 Torr (compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04183743 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-2b2c3252d8e94c129613a018ee39ede4 |
| Source note | uspto-grants-1980_01 |