HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266941Generated: October 30, 2026
Carbon Dioxide → Methyl 3-iso-pentyloxy-5-nitrobenzoate
https://huagongshe.com/reaction/2266941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-iso-Pentyloxy-5-nitrobenzoic acid | HCID 58060837 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-iso-pentyloxy-5-nitrobenzoate | HCID 66679881 | — |
Reaction Steps
In a three-neck reaction flask with a reflux condensor attached to 2 gas wash bottles, the second one filled with NaOH(aq) for absorption of developing CO2 and SO2, 3.7 g (14.6 mmol) 3-iso-pentyloxy-5-nitrobenzoic acid (10) were dissolved in methanol and cooled to 0° C., then 1.6 mL (21.9 mmol) thionyl chloride were added dropwise under stirring. The mixture was refluxed for 4 h, then stirred overnight at r.t.. It was concentrated, then repeatedly taken up in methanol and concentrated again, and put under vacuum. Finally, 2.97 g (76%) of a red-brown liquid, which was found to be sufficiently pure by NMR, were obtained. 1H NMR (CDCl3) δ 8.44 (dd, J1=1.4 Hz, J2=2.2 Hz, 1H), 7.88 (t, J1=2.2 Hz, J2=2.2 Hz, 1H), 7.87 (dd, J1=1.4 Hz, J2=2.2 Hz, 1H), 4.41 (t, J=6.8 Hz, 2H, PhOCH2CH2CH(CH3)2), 3.94 (s, 3H, OCH3), 1.88-1.65 (m, 3H), 0.99 (d, J=6.6 Hz, 6H, CH(CH3)2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858737B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-417ba3e960704f95a1837f721e8e608c |
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| Source note | uspto-grants-2010_12 |
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