HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399524Generated: October 31, 2026
4-Nitrobenzoic Acid → HCID 67639590, compound
https://huagongshe.com/reaction/399524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzoic Acid | HCID 6108 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid | HCID 88804 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 67639590 | HCID 67639590 | 77% |
Reaction Steps
To a solution of (4R)-1-(tert-butyloxycarbonyl)-4-hydroxy-L-proline (500 mg, 1.74 mmol) in benzene (20 mL) were added triphenylphosphine (548 mg, 2.09 mmol), p-nitrobenzoic acid (349 mg, 2.09 mmol), and diethyl azodicarboxylate (364 mg, 2.09 mmol). The reaction mixture was stirred for 1 hour at 80° C. and then evaporated. Flash silica gel chromatography eluting with 0.5% methanol/dichloromethane gave the desired product in 77% yield (581 mg). 400 MHz 1H NMR (CDCl3): δ1.38-1.47 (3s, 18H); 2.37 (m, 1H); 2.49-2.61 (m, 1H); 5.53 (m, 1H); 8.16-8.27 (m, 4H, Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05821261 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-05c38b36578f48dcb6b8b21b773b71d0 |
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| Source note | uspto-grants-1998_10 |
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