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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257131Generated: October 26, 2026

2,6-Lutidine → Benzo[d][1,2,3]thiadiazole-7-carbaldehyde

https://huagongshe.com/reaction/257131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
Reactant1,2,3-Benzothiadiazole-7-carbonyl chlorideHCID 18377607—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzo[d][1,2,3]thiadiazole-7-carbaldehydeHCID 14835681—

Reaction Steps

99 g of benzo-1,2,3-thiadiazole-7-carboxylic acid chloride are dissolved in 1.2 l of ethyl acetate, the mixture is treated at 0°-5° C. with a solution of 58.7 g of 2,6-lutidine in 200 ml of tetrahydrofuran as well as 33 g of palladium/charcoal catalyst (5% Pd), and hydrogenated under low pressure (104Pa) with a further addition of a total of 57 g of palladium/charcoal catalyst and 500 ml of tetrahydrofuran in 5 portions. The catalyst is subsequently removed by filtration and washed with tetrahydrofuran, and the filtrate is evaporated. The residue is purified on silica gel (CH2Cl2) and gives the title compound of m.p. 134°-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260423
Source datasetuspto-grants-1993_11
ORD IDord-d433502191674bf18c619faa0ceef992
Source noteuspto-grants-1993_11