HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 1-{[(Benzyloxy)(formyl)amino]methyl}cyclohexane-1-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-{[(Benzyloxy)amino]methyl}cyclohexane-1-carboxylic acid | HCID 71416983 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-{[(Benzyloxy)(formyl)amino]methyl}cyclohexane-1-carboxylic acid | HCID 58016118 | — |
Reaction Steps
To a cold solution of formic acid (15.3 mL, 0.4 mol) in dichloromethane (100 mL) at 0° C. under a nitrogen atmosphere was added acetic anhydride (5.75 mL, 60 mmol). After 1 h, a solution of 1-(benzyloxyamino-methyl)-cyclohexanecarboxylic acid from Preparation 19 (4.41 mmol theoretical) in dichloromethane (50 mL) was added. The mixture was stirred at room temperature for 18 h and was concentrated in vacuo. Brine (100 mL) was added and the mixture was extracted with dichloromethane (100 mL×2). The combined organic extracts were dried (MgSO4) and were evaporated in vacuo to yield the title compound as a pale, orange oil (1.77 g, 100%). MH+292.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07332485B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-1fa3d1f442664c35a64d7a4cba9c3d6f |
| Source note | uspto-grants-2008_02 |