HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(4-{[(Benzyloxy)carbonyl]amino}butyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(4-Aminobutyl)benzoic acid | HCID 22179973 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-{[(Benzyloxy)carbonyl]amino}butyl)benzoic acid | HCID 22179964 | 98% |
Reaction Steps
Sodium hydrogencarbonate (0.95 g, 11.32 mmol) was added into a suspension of 30 in THF (120 mL), followed by water (10 mL), affording a clear solution. Benzyl chloroformate (1.21 mL, 8.49 mmol) was then added into the reaction mixture at 0° C. The reaction mixture was then stirred at room temperature overnight. After that, the solvent was removed under reduced pressure. Ethyl acetate (70 mL) was added to the residue and the solution was washed with 2N HCl (2×30 mL) and water (2×50 mL), then dried in vacuum. 1.82 g (98%) of 31 was obtained as a white solid. 1H NMR (300 MHz, DMSO-d6) δ 1.11 (m, 2H), 1.28 (m, 2H), 2.33 (m, 2H), 3.02 (m, 2H), 5.01 (m, 2H), 7.15 (m, 7H), 7.93 (d 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820678B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-f8b8654b184e4c4ca06799d753c284f1 |
| Source note | uspto-grants-2010_10 |