HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60698Generated: October 29, 2026
4-Nitrobenzoic Acid → HCID 121396359, compound
https://huagongshe.com/reaction/60698
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrobenzoic Acid | HCID 6108 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 121396363 | HCID 121396363 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 121396359 | HCID 121396359 | 70.9% |
Reaction Steps
To a stirred solution of (1R)-1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]propan-1-ol (compound 6c, 50 g, 245 mmol), triphenylphosphine (195 g, 743 mmol), 4-nitrobenzoic acid (124 g, 743 mmol) in THF (1200 mL) was added diethyl azodicarboxylate (130 g, 743 mmol) dropwise at 0° C. under N2. After being stirred at 18° C. for 10 hours, the mixture was quenched by addition of saturated NaHCO3 solution and extracted with EtOAc. The organic layers were combined, dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica gel (eluting with 1:3 EtOAc in petroleum ether) to afford 61 g of [(1S)-1-[(3aR,5S,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]propyl] 4-nitrobenzoate (compound 6d) as a slight yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09441008B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-08163273cf64431593e3ec59ae2814aa |
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| Source note | uspto-grants-2016_09 |
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