HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979588Generated: October 25, 2026
Hexamethylenetetramine → Benzo(b)thiophene-5-carboxaldehyde
https://huagongshe.com/reaction/979588
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Methylbenzo(b)thiophene | HCID 84346 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Benzo(b)thiophene-5-carboxaldehyde | HCID 139097 | 297.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04668697 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-dbb990442d21427194cccc45d6fce2bb |
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| Source note | uspto-grants-1987_05 |
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