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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632709Generated: October 29, 2026

Sodium borohydride → 3-(4-Bromophenoxy)-6-methoxybenzo[b]thiophene 1,1-dioxide

https://huagongshe.com/reaction/632709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Bromo-3-(4-bromophenoxy)-6-methoxybenzo[b]thiophene 1,1-dioxideHCID 86730636—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
Product3-(4-Bromophenoxy)-6-methoxybenzo[b]thiophene 1,1-dioxideHCID 8673063797%

Reaction Steps

To a solution of 2-bromo-3-(4-bromophenoxy)-6-methoxy-benzo[b]thiophene 1,1-dioxide (3.10 g, 6.95 mmol) in MeOH (10 mL) and DMSO (30 mL) was added NaBH4 (0.789 g, 20.85 mmol). The mixture was stirred at room temperature for 3 h after which time the reaction was quenched with water and diluted with DCM. The organic layer was collected (phase separator) and concentrated to provide 3-(4-bromophenoxy)-6-methoxybenzo[b]thiophene 1,1-dioxide (2.47 g, 6.73 mmol, 97% yield) as an off white solid which was used without further purification. 1H NMR (400 MHz, CDCl3) δ ppm=3.85 (s, 3 H), 5.38 (s, 1 H), 7.02-7.08 (m, 3 H), 7.22 (d, J=2.53 Hz, 1 H), 7.47-7.60 (m, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321746B2
Source datasetuspto-grants-2016_04
ORD IDord-5d5e9bbfe8994e399e90ab796892a33a
Source noteuspto-grants-2016_04