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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007945Generated: October 30, 2026

Hexamethylenetetramine → Benzo(b)thiophene-6-carboxaldehyde

https://huagongshe.com/reaction/1007945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylenetetramineHCID 4101—
ReactantBenzoyl PeroxideHCID 7187—
ReactantMethylbenzothiopheneHCID 35790—
ReactantN-bromobutanimideHCID 67184—
ReactantBenzo(b)thiophene, 4-methyl-HCID 84345—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductBenzo(b)thiophene-6-carboxaldehydeHCID 138740—
Product1-Benzothiophene-4-carbaldehydeHCID 13985797—

Reaction Conditions

Temperature50 °C

Reaction Steps

In 350 mL of benzene is dissolved 23.53 g of a mixture of 4-methylbenzo[b]thiophene and 6-methylbenzo[b]thiophene, to which are added 0.77 g of benzoyl peroxide and 39.56 g of N-bromosuccinimide. The mixture thus formed is heated under reflux for 2 hours. After cooling the mixture to 50° C., 70 mL of acetic acid, 70 mL of water and 44.51 g of hexamethylenetetramine are added, and the mixture thus formed is heated under reflux for 2 hours. The solvent is distilled off under reduced pressure, the residue is mixed with water and ethyl acetate, and pH is adjusted to 7.5 with potassium carbonate. The organic layer is separated, washed with water and saturated aqueous solution of sodium chloride successively, and dried over anhydrous magnesium sulfate. The solvent is distilled off under reduced pressure, and the residue is purified by column chromatography (eluent: hexane:ethyl acetate=19:1 to 15:1). Thus, 5.24 g of benzo[b]thiophene-4-carboaldehyde, 5.09 g of benzo[b]thiophene-6-carboaldehyde and 6.71 g of mixture thereof are obtained as oily products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797726B1
Source datasetuspto-grants-2004_09
ORD IDord-0538278b67334cb6b939d5215e9728cf
Source noteuspto-grants-2004_09