HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Cbz-leucinal diethylacetal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | N-carbobenzoxy-L-leucinal | HCID 10911911 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Cbz-leucinal diethylacetal | HCID 54072519 | — |
Reaction Steps
104 mL of triethyl orthoformate was added over a period of 30 min to a solution of CBZ-Leu-H (12 g) and p-toluenesulfonic acid (0.9 g) in 100 mL of anhydrous ethanol (EtOH). The mixture was stirred for 30 min, and then was evaporated and diluted with 500 mL of ether. The ether layer was washed consecutively with saturated solutions of NaHCO3 and sodium chloride. The yellowish brown semisolid was recrystallized from cold hexane to yield off-white needles of CBZ-Leucinal diethylacetal. 1H NMR (300 MHz, CDCl3) δ: 7.28(m, 5H), 5.03(s, 2H), 4.77(d, 1H), 4.27(d, 1H), 3.8(m, 1H), 3.63(m, 2H), 3.43(m, 2H), 1.6(dd, 2H), 1.30(m, 2H), 1.12(m, 6H), 0.83(d, 6H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05614649 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-392f9cdb9f4d4cb48789b90b5e6d6823 |
| Source note | uspto-grants-1997_03 |