HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970659Generated: October 28, 2026
3-Aminobenzyl alcohol → HCID 59020664, compound
https://huagongshe.com/reaction/970659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminobenzyl alcohol | HCID 80293 | — |
| Reactant | HCID 72491609 | HCID 72491609 | — |
| Catalyst | Thiophenol | HCID 7969 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 59020664 | HCID 59020664 | 12.6% |
Reaction Steps
3-(3-(hydroxymethyl)phenylamino)-2-nitroacrylaldehyde (4.3 g, 19.4 mmol) was placed in 20 mL HOAc. 4.8 g of 3-aminobenzyl alcohol (4.8 g, 38.7 mmol) was dissolved in 5 mL conc HCl, then 20 mL HOAC was added to the HCl solution. This mixture was added to the reaction flask containing the 3-(3-(hydroxymethyl)phenylamino)-2-nitroacrylaldehyde in HOAc. The mixture was heated to reflux under nitrogen and after 20 min, benzene thiol (0.19 mL, 0.19 mmol) was added. The mixture was refluxed for 28 h (m/z=208.1). After allowing to cool, acid was removed under vacuum. The residue was dissolved in EtOAc/MeOH and loaded on a silica gel cartridge. Purification by column chromatography on silica gel using hexane/EtOAc (0-50%) then 10% MeOH/EtOAc as eluent gave the product (500 mg, 9%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312233B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-5d3b15ac6a434dddae4fe8e1babca4c7 |
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| Source note | uspto-grants-2007_12 |
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