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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194502Generated: October 31, 2026

P-Anisidine → HCID 14499218, compound

https://huagongshe.com/reaction/1194502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
Reactant2,6-DihydronaphthaleneHCID 14499217—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
ProductHCID 14499218HCID 1449921830%

Reaction Steps

A solution of 1.00 g (8.1 mmol, Aldrich) of p-anisidine, 5.20 g (32.5 mmol, 4 eq., Aldrich) of 2,6-dihydronaphthalene and 3.38 g (32.5 mmol, 4 eq., Aldrich) of sodium bisulfite in 60 ml of H2O was refluxed for 12 hours. The reaction was cooled to room temperature, extracted with EtOAc, dried (MgSO4) and concentrated in vacuo. Initial purification was accomplished via flash chromatography (1:6, 1:4 EtOAc/petroleum ether) and then concentration of appropriate fractions. Ethyl acetate was added, this was washed repeatedly with warm 0.1N NaOH to remove 2,6-dihydroxynaphthalene, dried (MgSO4) and concentrated in vacuo. Final purification by flash chromatography (1:4 THF/petroleum ether) yielded 633 mg (30%) of title compound as a muddy pink solid, m.p. 152°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814454
Source datasetuspto-grants-1989_03
ORD IDord-5736afd81bb8428c8cc0b80e5d785e8f
Source noteuspto-grants-1989_03