HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894350Generated: October 30, 2026
Potassium Carbonate → HCID 131712164, compound
https://huagongshe.com/reaction/894350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl L-phenylalaninate hydrochloride | HCID 75736 | — |
| Reactant | HCID 131712165 | HCID 131712165 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131712164 | HCID 131712164 | — |
Reaction Steps
A mixture of 0.759 g (0.0036 mole) of L-phenylalanine methyl ester hydrochloride and 40 ml of ethyl acetate was cooled in an ice-bath and 15 ml of cold 505 potassium carbonate solution was added. The mixture was equilibrated, and the ethyl acetate layer was separated and dried over anhydrous Na2SO4 at 0°. To the solution 1.129 g (0.003 mole) of the azlactone of N-carbobenzoxy-L-prolyl-dehydrophenylalanine was added. The reaction mixture was then refluxed for 8 hours, cooled and washed with N-hydrochloric acid, saturated sodium bicarbonate solution, saturated sodium chloride solution and dried over anhydrous Na2SO4. The solvent was evaporated in vacuo and the residual crystals were recrystallized from ethyl acetate/petroleum ether giving 1.473 g (88%) of N-carbobenzoxy-L-prolyl-dehydrophenylalanyl-L-phenylalanine methyl ester, mp 161°-163.5°, RfA 0.95, [α]D26 =-94.3° (c, 1% in EtOH); ir (CHCl3) 1735 (C=) 1690-1670 (C=O), 1630 cm-1 (C=C); NMR (CDCl3) δ1.5-2.4 (m, 4H, Pro ring), 3.0-3.33 (m, 2H, --CHCH2Ph), 3.33-3.57 (m, 2H, Pro ring) 3.63 (s, 3H, --COOCH3), 4.17-4.53 (m, 1H, --CH-CH2Ph), 4.67-5.0 (m, 1H, Pro ring), 5.02 (br.s., 2H>NOCOCH2Ph) 6.83-7.47 (m, 11H, ArH and PhCH=C<), 7.9-8.1 ppm (b, 2 H, NH, exchange by D2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04283328 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-3d87f89cbc7b4626b9319792f53dd237 |
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| Source note | uspto-grants-1981_08 |
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