HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178472436, compound → HCID 178472435, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178472436 | HCID 178472436 | — |
| Reactant | HCID 178511567 | HCID 178511567 | — |
| Product | HCID 178472435 | HCID 178472435 | — |
Reaction Steps
19.3 mL of concentrated hydrochloric acid (2.8 eq) was added to a solution of cis-4-aminocyclohexane carboxylic acid (10 g, 69.83 mmol) in anhydrous ethyl alcohol (250 mL). Mixture was stirred overnight at about 60° C. and then cooled to room temperature. Solvent was evaporated in vacuo. Crude material was then redissolved in acetonitrile, sonicated, and concentrated to a solid in vacuo. This acetonitrile wash was repeated three times to obtain 11.5 g of while solid (96% yield). Trans-ethyl 4-aminocyclohexanecarboxylate hydrochloride can be prepared following the same procedure using trans-4-aminocyclohexane carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187479B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-a424c350cc624310ba161085c814fd7c |
| Source note | uspto-grants-2015_11 |