HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Propanediamine → N-(2-Methyl-5-thiazolylmethyl]trimethylenediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Propanediamine | HCID 428 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(Chloromethyl)-2-methyl-1,3-thiazole | HCID 12808794 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2-Methyl-5-thiazolylmethyl]trimethylenediamine | HCID 14009896 | 89.9% |
Reaction Steps
Trimethylenediamine (37 g) was dissolved in 120 ml of acetonitrile, and a solution of 14.8 g of 5-chloromethyl-2-methylthiazole in 30 ml of acetonitrile was added dropwise at 10° to 15° C. After the addition, the mixture was stirred at 30° to 40° C. for a while, and then 8 g of a 50% aqueous solution of sodium hydroxide was added. Subsequently, the volatile materials were removed at a bath temperature of less than 50° C. under 5 mmHg. The inorganic materials were removed from the residue by filtration to give 16.7 g of N-(2-methyl-5-thiazolylmethyl)trimethylenediamine (purity about 90%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04845106 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-35b8cb5f2fe74c3ab6dea488ab149f84 |
| Source note | uspto-grants-1989_07 |