HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581725Generated: October 25, 2026
Water → 3-Bromobenzo[b]thiophene-5-carboxaldehyde
https://huagongshe.com/reaction/581725
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Benzo(b)thiophene-5-carboxaldehyde | HCID 139097 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromobenzo[b]thiophene-5-carboxaldehyde | HCID 18691608 | — |
Reaction Steps
To a solution of 3 g of benzo[b]thiophene-5-carbaldehyde in 30 ml of acetic acid is dropwise added 1.43 ml of bromine with ice-cooling. The temperature of the reaction mixture is elevated to room temperature, at which temperature the mixture is stirred for three hours. After the reaction, 50 ml of water and 50 ml of ethyl acetate are added to the thus stirred reaction mixture, and the resulting organic layer was separated, washed successively with water, a saturated aqueous sodium hydrogencarbonate solution and a saturated saline solution and then dried over anhydrous magnesium sulfate. Thereafter, the solvent is removed from the thus dried layer by distillation under reduced pressure. The residue obtained is purified by a moderate pressure column chromatography [eluent:hexane:ethyl acetate=20:1], to obtain 4.2 g of 3-bromobenzo[b]thiophene-5-carbaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922721 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-e56dfd084e2c48d28e927999c80e19bf |
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| Source note | uspto-grants-1999_07 |
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