HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746599Generated: October 29, 2026
Benzo(B)Thiophene → HCID 58591561, compound
https://huagongshe.com/reaction/746599
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzo(B)Thiophene | HCID 7221 | — |
| Reactant | 2-Bromoethyldimethylammonium bromide | HCID 45791347 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58591561 | HCID 58591561 | 65% |
Reaction Steps
To a cooled (−78° C.) solution of benzothiophene (74.5 mmol) in anhydrous THF (100 mL) was added slowly n-BuLi (82 mmol, 1.6 M in hexanes). The mixture was stirred at −78° C. for 1 hr. β-Dimethylaminoethyl bromide hydrobromide (41 mmol) was added at −78° C. and the temperature was allowed to reach 0° C. over 5 hours. The mixture was quenched in sat. NH4Cl, the pH of the aqueous layer was adjusted to 7-8 with sat. NaHCO3, and the mixture was extracted with EtOAc (4×). The combined organic layers were concentrated and extracted with 1N HCl (3×). The combined HCl layers were made basic with sat. NaHCO3, extracted with EtOAc (4×), and the combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to afford Compound 1a (2-Benzo[b]thiophen-2-yl-ethyl)-dimethyl-amine (4.96 g, 65%) as a tan solid; MS (MH+)=206.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07393865B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-6d3d4bee1ea2456198465e9722e4f461 |
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| Source note | uspto-grants-2008_07 |
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