HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233628Generated: October 25, 2026
Dicyclohexylcarbodiimide → Methyl (R)-4-[(2-hydroxy-1-phenylethyl)amino]-4-oxo-2-butenoate
https://huagongshe.com/reaction/233628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (R)-beta-aminophenethyl alcohol | HCID 2724025 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | (E)-4-methoxy-4-oxobut-2-enoate | HCID 21721168 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl (R)-4-[(2-hydroxy-1-phenylethyl)amino]-4-oxo-2-butenoate | HCID 53871317 | — |
Reaction Steps
To a solution of monomethyl fumarate (3.0 g, 23 mmol) in ethyl acetate (40 mL) was added 1-hydroxybenzotriazole hydrate (3.0 g, 22 mmol), followed by N,N'-dicyclohexylcarbodiimide (4.5 g, 22 mmol) and the reaction stirred at ambient temperature for 1 hour. The solid was filtered off and discarded. To the filtrate was added (R)-α-phenylglycinol (3.0 g, 22 mmol ) and stirring continued for 20 minutes. The volatiles were removed in vacuo (40° C.) and the residue purified by flash chromatography on normal phase silica gel using hexane: ethyl acetate (1:1) as eluant. Recovered 2.5 g (46%) of (18) as a white solid, m.p. 75°-77° C.; IR (neat) 3250 (OH), 1729 (C=O ester), 1666 (C=O amide), 1640 (C=C)cm-1 ;NMR (CDCl3) δ 7.3-7.4 (5H, m, Ph), 7.0 (1H, d, J 15 Hz, trans alkene), 6.8 (1H, d, J 15 Hz, trans alkene), 6.6 (1H, br d, NH), 5.2 (1H, m, CH), 3.9 (2H, t, J 3 Hz, CH2), 3.8 (3H, s, CH3), 2.3 (1H, t, J 5 Hz, OH); [α]D -53° (CHCl3, 24° C., c=1); anal C13H15NO4 ; requires C 62.64% H 6.07% N 5.62%; found C 62.72% H 5.92% N 5.48%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05593967 |
|---|
| Source dataset | uspto-grants-1997_01 |
|---|
| ORD ID | ord-d97dbee2fa244c0bb9d07ea0152a6b60 |
|---|
| Source note | uspto-grants-1997_01 |
|---|