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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799069Generated: November 3, 2026

4-Hydroxybenzaldehyde → HCID 87309085, compound

https://huagongshe.com/reaction/1799069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChlorobenzothiazoleHCID 11987—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetonitrileHCID 6342—
ProductHCID 87309085HCID 87309085—

Reaction Steps

To a solution of 2-chlorobenzothiazole (33.7 g, 199 mmol) in CH3CN (500 mL) was added 4-hydroxy benzaldehyde (24.3 g, 199 mmol) and K2CO3 (28 g, 199 mmol). The heterogeneous mixture was heated at reflux for 72 h and then cooled to rt. The solids were removed by filtration and washed with CH3CN (100 mL). To the filtrate was added an aqueous solution of NaHSO3 (26 g, 199 mmol, 66 mL water). After stirring for 3.5 h, the mixture was filtered and the wet cake was dried under vacuum overnight to afford the bisulfite complex (66 g, 92%) as a white powder. 1H NMR (500 MHz, DMSO-d6): 7.93 (d, J=8.0 Hz, 1H), 7.74 (d, J=8.0 Hz, 1H), 7.60-7.55 (m, 2H), 7.44-7.39 (m, 1H), 7.35-7.29 (m, 3H), 6.03 (d, J=5.2 Hz, 1H), 5.04 (d, J=5.2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344008B2
Source datasetuspto-grants-2013_01
ORD IDord-c872e3b30a034e7e9974085244dfdc2a
Source noteuspto-grants-2013_01