HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethanol → HCID 131712944, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 20512409 | HCID 20512409 | — |
| Product | HCID 131712944 | HCID 131712944 | 34.3% |
Reaction Steps
1.5 ml (1.8 g, 0.022 moles) of ethylene chlorohydrine and 0.35 g (0.002 moles) of potassium iodide are added to a solution of 6.14 g (0.02 moles) of 1,3-bis(2',6'-dimethylphenyl)-2-imino-4-methyl-imidazolidine, obtained as described in Example 3, in 60 ml of dry dimethylformamide. The resulting mixture is stirred at 100° to 105° C. for 6 hours, thereafter it is poured onto 300 ml of icy water. The separated product is filtered off, washed with water and ethyl acetate, and dried. 1.6 g of 1,3-bis(2',6'-dimethylphenyl)-2-(β-hydroxyethyl)-imino-4-methyl-imidazolidine hydrochloride are obtained; m.p.: 288°-291° C. (after recrystallization from a 6:4 mixture of methanol and water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04369325 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-09da78afeebf42a2bb0ce63d4f09e3f1 |
| Source note | uspto-grants-1983_01 |