HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122169Generated: October 29, 2026
1-(Methoxymethyl)-3-nitrobenzene → 3-(Methoxymethyl)aniline
https://huagongshe.com/reaction/2122169
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Methoxymethyl)-3-nitrobenzene | HCID 11389609 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(Methoxymethyl)aniline | HCID 13042032 | 99.1% |
Reaction Steps
EX-514B) The 3-(methoxymethyl)nitrobenzene (4.18 g, 25 mmol) from EX-514A was dissolved in 160 mL of acetic acid. Zinc dust (5 g, 76.5 mmol) was added, and the solution was stirred at room temperature for 18 hours, at which time HPLC analysis indicated that no 3-(methoxymethyl)nitrobenzene starting material remained. The reaction mixture was filtered through celite and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with aqueous saturated sodium bicarbonate. The organic layer was washed with water, then dried over MgSO4, and concentrated in vacuo to give 3.4 g (99%) of the desired 3-(methoxymethyl)aniline as a brown oil. The crude product was used without further purification. HRMS calcd. for C8H12NO: 138.0919 [M+H]+, found: 138.0929. 1H NMR (CDCl3) δ3.4 (s, 3H), 3.7 (s, 2H), 4.4 (s, 2H), 6.6 (d, 1H), 6.7 (m, 2H), 7.2 (t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696472B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-f2c880637e704bbaac6925aa1816ef6a |
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| Source note | uspto-grants-2004_02 |
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