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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585734Generated: November 1, 2026

Vanillin → 24033-07-6

https://huagongshe.com/reaction/1585734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantDiethyl EtherHCID 3283—
ReactantP-AnisidineHCID 7732—
ReactantEthyl acetate hexaneHCID 21226206—
SolventMethanolHCID 887—
Product24033-07-6HCID 681370—

Reaction Steps

3-Methoxy-4-hydroxybenzaldehyde (vanillin, 1 g, 6.57 mmol) was dissolved in methanol (30 ml). To this solution was added p-anisidine (0.810 g, 6.57 mmol) and the resultant reaction solution was stirred overnight under nitrogen at room temperature. The reaction solution was taken to dryness in vacuo with the application of heat. The resultant solid was azeotropically mixed with methanol (2x), ether (1x), and again with methanol (2x) to yield yellow crystals. The crystals were triturated with hot ether to yield the title product: 1H NMR (300 MHz, CDCl3); δ 8.36 (S, 1H), 7.60 (S, 1H), 7.30-7.17 (m, 3H), 7.05-6,91 (m, 3H), 6.10 (S, 1H), 3.97 (S, 3H), 3.83 (S, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939460
Source datasetuspto-grants-1999_08
ORD IDord-1e2f7b934bc244598df4f763b1bffd6b
Source noteuspto-grants-1999_08