HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 3-(azidomethyl)cyclobutanecarboxylate → 3-(Aminomethyl)cyclobutanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 3-(azidomethyl)cyclobutanecarboxylate | HCID 86660436 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Aminomethyl)cyclobutanecarboxylic acid | HCID 58557901 | 102.6% |
Reaction Steps
To a flask charged with 10% palladium on carbon (0.20 g, 0.19 mmol) was added a solution of benzyl 3-(azidomethyl)cyclobutanecarboxylate (2.00 g, 8.15 mmol, prepared using IIII from benzyl 3-(hydroxymethyl)cyclobutanecarboxylate (Parkway Scientific), JJJJ with sodium azide) in MeOH (100 mL). The reaction mixture was sparged with hydrogen and an atmosphere of hydrogen was maintained via a balloon. The reaction mixture was stirred for about 4 h at ambient temperature and then was filtered through a pad of Celite®, washed with MeOH and concentrated in vacuo to give the crude 3-(aminomethyl)cyclobutanecarboxylic acid (1.08 g, 100%) which was used without further purification: LC/MS (Table 1, Method r) Rt=2.41 min (ELSD); MS m/z: 130 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426411B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-9b7c3b3abd3a4d9eb3793ae880d10f5a |
| Source note | uspto-grants-2013_04 |