HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 1-Benzylazetidine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Disodium | HCID 141233 | — |
| Reactant | 1-benzylazetidine-3,3-dicarboxylic Acid | HCID 11310885 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | o-Tolylacetic acid | HCID 69519 | — |
| Product | 1-Benzylazetidine-3-carboxylic acid | HCID 3161318 | — |
Reaction Steps
A mixture of the disodium salt of N-benzylazetidine-3,3-dicarboxylic acid and sodium carbonate (approximately 2:1 by weight, total weight 7.5 g) were dissolved in 100 ml of a toluene-acetic acid mixture (2/1, v/v), with immediate evolution of carbon dioxide from the sodium carbonate. The mixture was warmed and stirred, and then refluxed over a Dean and Stark water separator. After 1/2 hour evolution of carbon dioxide had ceased and 1.5 ml of an acetic acid-water mixture had separated. The slightly hazy solution was cooled to room temperature. A white fluffy solid comprising sodium acetate (3.6 ) g) was removed by filtration. Distillation of the clear filtrate yielded 4.5 g of N-benzyl-3-carboxy-azetidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04778577 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-26b063d4bc754f12a182ebb4d9486f70 |
| Source note | uspto-grants-1988_10 |