HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → HCID 13730776, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Quinaldic Acid | HCID 7124 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-2,3-dimethylbutanamide | HCID 9793773 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13730776 | HCID 13730776 | 87% |
Reaction Steps
To a solution of quinaldic acid (20 g, 0.116 mol) in tetrahydrofuran (500 ml) cooled to -9° C. is added methyl chloroformate (8.92 ml, 0.116 mol) followed by triethylamine (18.4 ml, 0.139 mol). After 20 minutes 2-amino-2,3-dimethylbutyramide (15.1 g, 0.116 mol) is added and the mixture stirred overnight at room temperature. Water is added and the solution is reduced to 200 ml of a rotorvap. A white solid separates and is filtered off, water washed and dried. Recrystallization from absolute ethanol gives the product mp 179°-180° C., 26.86 g (87%). Anal. calcd. for C16H19N3O2 : C, 67.34; H, 6.73; N, 14.72. Found: C, 67.14; H, 6.17; N, 14.72.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04638068 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-4c39f58aaef4420f8d2fd5a895649612 |
| Source note | uspto-grants-1987_01 |