HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371005Generated: October 31, 2026
Boron → 6,7-Dichloro-5-methoxy-2-n-propylbenzo[b]thiophene
https://huagongshe.com/reaction/371005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron | HCID 5462311 | — |
| Reactant | HCID 13290182 | HCID 13290182 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6,7-Dichloro-5-methoxy-2-n-propylbenzo[b]thiophene | HCID 13952871 | 75.1% |
Reaction Steps
To a mixture of 44 g of 6,7-dichloro-2,3-dihydro-3-hydroxy-5-methoxy-2-n-propylbenzo[b]thiophene in 275 ml of glacial acetic acid is added 65 ml of boron triluoride etherate and the mixture is warmed on a steam bath until it becomes clear. The solution is stired for 10 mins and then quenched with a mixture of 500 g of ice and 200 ml of a 10% sodium hydroxide solution. The mixture is neutralized with 50% sodium hydroxide solution and then extracted with two 300-ml portions of ethyl ether. The organic layers are combined, washed with 100 ml of a saturated sodium bicarbonate solution, 100 ml of water, dried over anhydrous magnesium sulfate, filtered and the solvent is removed to give an oil. Chromatography of the oil on an alumina column using 9:1-hexane:ethyl ether as eluting solvent gives 31 g of 6,7-dichloro-5-methoxy-2-n-propylbenzo[b]thiophene as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04528399 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-623363c524ab463781b86bc90db63f16 |
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| Source note | uspto-grants-1985_07 |
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