HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylbenzylamine → HCID 13912532, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylbenzylamine | HCID 6993 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,5-Dimethyl-4-nitrobenzoic acid | HCID 249413 | — |
| Reactant | 3,5-Dimethyl-4-nitrobenzoyl chloride | HCID 12332131 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13912532 | HCID 13912532 | — |
Reaction Steps
A solution of 3,5-dimethyl-4-nitrobenzoyl chloride in tetrahyrofuran, generated from 7.0 g of 3,5-dimethyl-4-nitrobenzoic acid by standard procedures, was added to 4.3 g of 2-methylbenzyl amine and 5.0 ml of triethylamine in tetrahydrofuran. The reaction was stirred at ambient temperature overnight, chilled, and filtered. The filtrate was evaporated in vacuo and the residue therefrom was dissolved in chloroform, washed sequentially with 1N hydrochloric acid, 1N sodium hydroxide, water, and a saturated sodium chloride solution, dried over sodium sulfate, filtered, and evaporated in vacuo. Crystallization from methanol/water provided 4.7 g of the desired title product, m.p. 202°-203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04684748 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-5f1172c237c240db90b4e91212b88ef5 |
| Source note | uspto-grants-1987_08 |