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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616785Generated: November 3, 2026

Vanillin → HCID 965934, compound

https://huagongshe.com/reaction/1616785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromomethylnaphthaleneHCID 70320—
SolventAcetoneHCID 180—
ProductHCID 965934HCID 96593476.3%

Reaction Steps

2-(Bromomethyl)naphthalene (1.3 g, 5.9 mmol) was added to a suspension of vanillin (0.60 g, 3.9 mmol) and potassium carbonate (1.6 g, 12 mmol) in acetone (10 mL) and treated according to Procedure 3. The crude product was recrystallised from EtOAc/petrol providing 3-methoxy-4-(naphth-2-ylmethoxy)benzaldehyde (0.87 g, 75%) as a colourless crystalline solid; mp 107-108° C.; δH (400 MHz, CDCl3) 3.97 (s, 3H, OCH3), 5.41 (s, 2H, OCH2), 7.38 (m, 1H, Naphth-H), 7.44 (d, J2,6=1.6 Hz, 1H, H2), 7.48-7.50 (m, 3H, H6, Naphth-H), 7.55 (m, 1H, Naphth-H), 7.83-7.89 (m, 4H, Naphth-H), 9.84 (s, 1H, CHO); δC (100 MHz, CDCl3) 56.3, 71.3 109.7, 112.8, 125.1 126.4, 126.5, 126.6, 126.8, 128.0, 128.2, 128.9, 130.6, 133.4, 133.5, 133.7, 150.4, 153.8, 191.1; vmax 991, 1131, 1263, 1505, 1580, 1672, 2884 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765812B2
Source datasetuspto-grants-2014_07
ORD IDord-f871a746e2f5428a9d678ea9f7c327a8
Source noteuspto-grants-2014_07