HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → cis-2-Aminocyclohexanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | methyl (1R,2S)-2-aminocyclohexanecarboxylate | HCID 24751169 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | cis-2-Aminocyclohexanecarboxamide | HCID 2724813 | — |
Reaction Steps
cis-2-Aminocyclohexanecarboxylic acid methyl ester (2.20 g, 14.0 mmol) was treated with aqueous ammonium hydroxide (40 mL) in toluene (40 mL) and stirred vigorously at room temperature for 16 h. The reaction was concentrated to dryness in vacuo and azeotroped with toluene (50 mL). The crude product, cis-2-aminocyclohexanecarboxylic acid amide, was used in the next reaction without purification: 1H NMR (400 MHz, DMSO-d6) δ 7.78 (2 H, s br), 7.67 (s, 1 H), 7.25 (s, 1 H), 1.87 (m, 2 H), 1.60 (m, 4 H), 1.41 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084178B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-fc1c3c23629140928ac9e042705804cc |
| Source note | uspto-grants-2006_08 |