HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892090Generated: October 25, 2026
Sodium Hydroxide → Aniline 3-hydroxymethyl-4-methoxyaniline
https://huagongshe.com/reaction/892090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2-Methoxy-5-nitrophenyl)methanol | HCID 17604241 | — |
| Reactant | Tin dichloride dihydrate | HCID 43835034 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Aniline 3-hydroxymethyl-4-methoxyaniline | HCID 86589140 | 293.6% |
Reaction Steps
A mixture of 2-methoxy-5-nitrobenzylalcohol (1.02 g, 6.03 mmol) and SnCl2.H2O (6.8 g, 30.15 mmol) in EtOH (20 mL) was heated at 70° C. for 1 hour. After cooling, the mixture was treated with 2M NaOH and extracted with ether. The organic layer was washed with water, dried, and evaporated under vacuum to provide 2.18 g (84%) of the aniline 3-hydroxymethyl-4-methoxyaniline: 1H NMR (DMSO-d6, 500 MHz) δ 6.66 (d, 1H, J=2.2 Hz), 6.61 (d, 1H, J=8.6 Hz), 6.38 (dd, 1H, J=2.4 and 8.2 Hz), 4.81 (t, 1H, J=5.5 Hz), 4.54 (br, 2H), 4.37 (d, 2H, J=5.8 Hz), 3.61 (s, 3H). 3-hydroxymethyl-4-propyloxyaniline
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005445B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-f3222daecaa54220bc17b768e99eeb7f |
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| Source note | uspto-grants-2006_02 |
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