HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 1-[3-(benzylamino)-4-fluorobenzyl]cyclopropanecarboxylate → tert-Butyl 1-(3-amino-4-fluorobenzyl)cyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 1-[3-(benzylamino)-4-fluorobenzyl]cyclopropanecarboxylate | HCID 58136659 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 1-(3-amino-4-fluorobenzyl)cyclopropanecarboxylate | HCID 58136688 | — |
Reaction Steps
145.0 g (407.9 mmol) of tert-butyl 1-[3-(benzylamino)-4-fluorobenzyl]cyclopropanecarboxylate were dissolved in 1450 ml of ethanol, and 9.67 g of palladium hydroxide (20% on carbon) were added. The suspension was stirred at RT under a hydrogen atmosphere at standard pressure for 18 h. The reaction mixture was then filtered off with suction through kieselguhr, and the filtrate was concentrated. After drying under high vacuum, 500 ml of pentane were added to the residue, resulting in the precipitation of the product. The suspension was stirred in an ice bath for 1 h. The solid was then filtered off with suction, washed twice with pentane and dried under high vacuum. 88.5 g (73.6% of theory) of the title compound were thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309198B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-e9932671c9f54a9aa732e04f2d3b85a2 |
| Source note | uspto-grants-2016_04 |