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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213992Generated: October 27, 2026

2-(5-Methoxy-2-methoxymethoxyphenyl)-4-methylbenzoxazole → 2-(4,5-Dimethoxy-2-methoxymethoxyphenyl)-4-methylbenzoxazole

https://huagongshe.com/reaction/2213992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-Methoxy-2-methoxymethoxyphenyl)-4-methylbenzoxazoleHCID 21959325—
Reactant2-[(4-Methoxymethoxybenzylidene)amino]-3-methylphenolHCID 21959327—
Product2-(4,5-Dimethoxy-2-methoxymethoxyphenyl)-4-methylbenzoxazoleHCID 21959318—

Reaction Steps

2-(4,5-dimethoxy-2-methoxymethoxyphenyl)-4-methylbenzoxazole (F9) was prepared in a similar manner for the preparation of 2-(5-methoxy-2-methoxymethoxyphenyl)-4-methylbenzoxazole (F8) by using 2-[(4-methoxymethoxybenzylidene)amino]-3-methylphenol (F6) (3.31 g, 10 mmol) instead of 2-[(5-methoxy-2-methoxymethoxybenzylidene)amino]-3-methylphenol (F4) in 62% (2.07 g): 1H-NMR (400 MHz, CDCl3) δ2.66 (s, 3H), 3.58 (s, 3H), 3.95 (s, 3H), 3.97 (s, 3H), 5.28 (s, 2H), 6.84 (s, 1H), 7.12 (d, 1H, J=8.0 Hz), 7.21 (t, 1H, J=8.0 Hz), 7.39 (d, 1H, J=8.0 Hz), 7.63 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105680B1
Source datasetuspto-grants-2006_09
ORD IDord-f9c657ccb22046d28d0b16c2c22082b3
Source noteuspto-grants-2006_09