HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Aminocyclopropane-1-carboxylic acid → 1-[(Cyclohexylcarbonyloxyethoxy)carbonylamino]cyclopropanecarboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Aminocyclopropane-1-carboxylic acid | HCID 535 | — |
| Reactant | (2,5-Dioxoazolidinyloxycarbonyloxy)ethyl cyclohexanecarboxylate | HCID 86618759 | — |
| Product | 1-[(Cyclohexylcarbonyloxyethoxy)carbonylamino]cyclopropanecarboxylic Acid | HCID 24798322 | 16.4% |
Reaction Steps
Following the general procedure for the synthesis of acyloxyalkyl carbamates, ACPC (426 mg, 4.2 mmol) and (2,5-dioxoazolidinyloxycarbonyloxy)ethyl cyclohexanecarboxylate (1.1 g, 3.5 mmol) were reacted to provide 172 mg (16% yield) of the title compound (10) as a white powder after work-up and mass-guided preparative HPLC purification. M.p.: 123.6-125.3° C. 1H NMR (CDCl3, 400 MHz): δ=9.92 (br s, 1H), 6.76 (q, 1H), 6.34 (br s, 0.3H), 5.59 (s, 0.7H), 2.27 (m, 1H), 1.10-1.95 (m, 17H). MS (ESI) m/z 317.15 (M+NH4)+; 322.13 (M+Na)+; 298.15 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07799829B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-e1f57fad8cbf4e20a06f286bbe15d66d |
| Source note | uspto-grants-2010_09 |