HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494887Generated: October 30, 2026
Phosphoric Acid → 5-Bromo-1-benzothiophene
https://huagongshe.com/reaction/494887
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | 1-Bromo-4-[(2,2-diethoxyethyl)sulfanyl]benzene | HCID 11833671 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 5-Bromo-1-benzothiophene | HCID 2776578 | — |
Reaction Steps
5-Bromobenzo[b]thiophene (Chemical Abstracts number 4923-87-9) was prepared as described in Banfield et al.; J. Chem. Soc.; 1956; 2603-2607, and in Seed, Alexander J.; et al. J. Mater. Chem.; vol10; 2000; 2069-2080. A mixture of phosphoric acid (218 g) and chlorobenzene (2 L) was heated at 130° C. and then treated with the product from Example 165A (107.0 g) over 2 hours using a syringe pump. The mixture was heated at 130° C. for 15 hours. Dean-Stark trap was used at the beginning of the reflux to remove water from the mixture. The mixture was allowed to cool to room temperature and quenched with 400 mL of water. The bottom aqueous layer was extracted with 200 mL of methylene chloride. The combined organic layer was washed with 200 mL of 10% Na2CO3, and concentrated to brown oil (129.4 g). The crude oil was dissolved in 1 L of 10:90 EtOAC:hexane, filtered through a short pad of silica gel and concentrated to a yellow oil (85.54 g, 95.8% yield). Further purification was done by column chromatography (silica gel, 5:95 EtOAc:hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538138B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-fca231b45cc04562b4f1a0fc8596efe3 |
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| Source note | uspto-grants-2009_05 |
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