Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Methoxymethyl)-3-nitrobenzeneHCID 11389609—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product3-(Methoxymethyl)anilineHCID 1304203299.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696472B2
Source datasetuspto-grants-2004_02
ORD IDord-f2c880637e704bbaac6925aa1816ef6a
Source noteuspto-grants-2004_02