HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189949Generated: October 29, 2026
HCID 19762862, compound → HCID 67296566, compound
https://huagongshe.com/reaction/1189949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19762862 | HCID 19762862 | — |
| Reactant | 3-(3-Aminophenyl)-3-hydroxypropanenitrile | HCID 59316960 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 67296566 | HCID 67296566 | — |
Reaction Steps
To a stirred solution of aniline 12 (1.0 g, 6.1 mmol) in EtOH:H2O (9:1) was added 2-propylpentyl 4-methylbenzenesulfonate (0.87 g, 3.08 mmol). The reaction mixture was heated under reflux for 4 days, concentrated under reduced pressure. The residue was diluted with water and extracted with EtOAc three times. Combined organic layers were dried over anhydrous sodium sulfate and concentrated under reduced pressure to dryness. Purification by flash chromatography (25% EtOAc—hexanes) gave 3-hydroxy-3-(3-(2-propylpentylamino)phenyl)propanenitrile as a colorless semi-solid. Yield (0.3 g, 18%); 1H NMR (400 MHz, CDCl3) δ 7.17 (t, J=7.6 Hz, 1H), 6.66 (d, J=7.6 Hz, 1H), 6.62 (d, J=2.0 Hz, 1H), 6.57 (dd, J=2.0, 8.0 Hz, 1H), 4.95 (dt, J=3.2, 6.0 Hz, 1H), 3.72 (bs, 1H), 3.02 (d, J=6.0 Hz, 2H), 2.80 (d, J=6.8 Hz, 2H), 2.89 (d, J=3.2 Hz, 1H), 1.64-1.57 (m, 1H), 1.37-1.20 (m, 8H), 0.84 (t, J=6.8 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674137B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-51f1b119d05548b68bc690914ca413f5 |
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| Source note | uspto-grants-2014_03 |
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