Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746599Generated: October 29, 2026

Benzo(B)Thiophene → HCID 58591561, compound

https://huagongshe.com/reaction/746599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
Reactant2-Bromoethyldimethylammonium bromideHCID 45791347—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58591561HCID 5859156165%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393865B2
Source datasetuspto-grants-2008_07
ORD IDord-6d3d4bee1ea2456198465e9722e4f461
Source noteuspto-grants-2008_07