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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979588Generated: October 25, 2026

Hexamethylenetetramine → Benzo(b)thiophene-5-carboxaldehyde

https://huagongshe.com/reaction/979588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylenetetramineHCID 4101—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methylbenzo(b)thiopheneHCID 84346—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
SolventChloroformHCID 6212—
ProductBenzo(b)thiophene-5-carboxaldehydeHCID 139097297.4%

Reaction Steps

Under N2, NBS (6 g, 0.034 mol) was added to a solution of 5-methylbenzo[b]thiophene (30.8 g, 0.21 mol), benzoylperoxide (1.6 g) in CCl4 (300 ml) and was heated at reflux. After 15 minutes, the remainder of the NBS (35 g, 0.2 mol) was added over a period of 5 minutes and heated at reflux for 1.5 hours. The reaction mixture was then cooled, filtered and the filtrate washed with H2O (2x), dried, filtered and concentrated to dryness. The residue was dissolved in CHCl3 (130 ml) and added to a solution of hexamethylenetetramine (33.6 g, 0.24 mol) in CHCl3 (60 ml). After 0.5 hour, the reaction mixture was cooled, filtered and the solid washed with hexane. After drying, the solid was dissolved in acetic acid-H2O (275 ml) and heated at reflux for 2 hours. Then concentrated HCl (55 ml) was added and the mixture refluxed an additional 5 minutes. After cooling, the solution was extracted with ether (3×), and the organic extracts were backwashed with saturated Na2CO3 (2×), dried, filtered, and concentrated to dryness to yield 16.4 g (48%) of product

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668697
Source datasetuspto-grants-1987_05
ORD IDord-dbb990442d21427194cccc45d6fce2bb
Source noteuspto-grants-1987_05