HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201683Generated: October 29, 2026
Sodium Carbonate → Tert-butyl (5-(cyclopent-1-en-1-yl)-2-nitrophenyl)carbamate
https://huagongshe.com/reaction/2201683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Trifluoro-methanesulfonic acid cyclopent-1-enyl ester | HCID 11769877 | — |
| Reactant | Tert-butyl (2-nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate | HCID 71007411 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl (5-(cyclopent-1-en-1-yl)-2-nitrophenyl)carbamate | HCID 71007338 | 32.2% |
Reaction Steps
To a solution of tert-butyl (2-nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate (16 g, 43.9 mmol, 1.0 equiv.) in 1,4-dioxane (320 mL) were added cyclopent-1-en-1-yl trifluoromethanesulfonate (11.4 g, 52.7 mmol, 1.2 equiv.), Pd (PPh3)4 (2.54 g, 2.2 mmol, 0.05 equiv.) and a solution of Na2CO3 (5.6 g, 52.7 mmol, 1.2 equiv.) in water (160 mL) at room temperature. The reaction was then heated to 110° C. and stirred for 4 h. The reaction mixture was filtered through celite then concentrated under reduced pressure. The crude residue was purified by column chromatography (silica gel, 2% EtOAc/hexanes) to give tert-butyl (5-(cyclopent-1-en-1-yl)-2-nitrophenyl)carbamate (4.3 g, 32% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365498B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-74050404db4243c2853e7943059a3cb2 |
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| Source note | uspto-grants-2016_06 |
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