HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467049Generated: October 30, 2026
HCID 66746823, compound → HCID 66746696, compound
https://huagongshe.com/reaction/1467049
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 66746823 | HCID 66746823 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Acetic acid tetrahydrofuran | HCID 23444217 | — |
| Product | HCID 66746696 | HCID 66746696 | 83% |
Reaction Steps
To a solution of 2-isobutoxy-6-nitrobenzonitrile (Example 41c, 34.3 g, 0.156 mol) in AcOH/THF (1:1 by volume, 250 mL) was added iron powder (17.36 g, 0.311 mol) in one portion. The stirred suspension was heated to reflux for 30 minutes. After it was cooled down to room temperature, the reaction solution was diluted with EtOAc (1 L). The solid was removed by filtration, and the filtrate was washed subsequently with water (300 mL×2), 1N NaOH (300 mL), saturated Na2CO3 aqueous solution (300 mL), brine (300 mL), and dried over Na2SO4. After evaporation of the solvent, the residue was purified by chromatography on silica gel eluting with 20% EtOAc in hexanes to give the title compound as a yellow oil (16.4 g, 83%). 1H NMR (400 MHz, DMSO-d6) δ 0.96 (d, J=6.8 Hz, 6H), 1.96-2.02 (m, 1H), 3.75 (d, J=6.4 Hz, 2H), 5.96 (s, 2H), 6.17 (d, J=8.4 Hz, 1H), 6.30 (d, J=8.4 Hz, 1H), 7.15 (t, J=8.8 Hz, 1H). MS 191 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000054B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-82edec2b4cc04857ab4923d68d80aad6 |
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| Source note | uspto-grants-2015_04 |
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