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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717361Generated: November 1, 2026

3,4,5-Trimethoxybenzaldehyde → HCID 178486783, compound

https://huagongshe.com/reaction/717361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantDimethylacetamideHCID 31374—
Reactant2-Amino-4,5-dimethoxybenzamideHCID 10867236—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
ProductHCID 178486783HCID 178486783—

Reaction Conditions

Temperature139 °C

Reaction Steps

Into a 500-mL 3-necked round-bottom flask, was placed 2-amino-4,5-dimethoxybenzamide (12 g, 61.16 mmol, 1.00 equiv), dimethylacetamide (200 mL), 3,4,5-trimethoxybenzaldehyde (12 g, 61.16 mmol, 1.00 equiv) and NaHSO3 (9.55 g, 91.83 mmol, 1.50 equiv). The resulting solution was stirred overnight at 139° C. The mixture was cooled to room temperature. The resulting solution was diluted with 800 mL of water. The solids were collected by filtration. The filter cake was washed with 1×100 ml of water, 100 ml of diethyl ether and 100 mL of methanol. This resulted in 12 g (53%) of 6,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)quinazolin-4-ol as a brown solid. MS (ESI) m/z 373 [M+h]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193707B2
Source datasetuspto-grants-2015_11
ORD IDord-c99429e3cc334846961346b74a8360c6
Source noteuspto-grants-2015_11