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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456292Generated: November 4, 2026

Monobenzone → HCID 15347456, compound

https://huagongshe.com/reaction/1456292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMonobenzoneHCID 7638—
ReactantBenzo(b)thiophene, 3-bromo-HCID 123250—
Solvent2,4,6-TrimethylpyridineHCID 7953—
SolventEthyl AcetateHCID 8857—
ProductBenzo(B)ThiopheneHCID 7221—
ProductHCID 15347456HCID 1534745635%

Reaction Steps

To a solution of 3-bromo-benzo[b]thiophene (69.62 g, 0.325 mol) in 55 mL of anhydrous collidine under N2 was added 4-benzyloxyphenol (97.6 g, 0.488 mol) and cuprous oxide (23.3 g, 0.163 mol). The mixture was heated to reflux for 24 hours. Upon cooling, the reaction mixture was diluted with ethyl acetate (200 mL) and the crude mixture filtered through a pad of Celite® (Aldrich, Milwaukee, Wis.) to remove inorganic salts. The filtrate was washed with 1N hydrochloric acid (3×150 mL). The organic was dried with sodium sulfate and concentrated in vacuo to a liquid. Thianaphthene was removed by distillation (10 mm Hg, 115°-120° C). The remainder of the material was chromatographed (silicon dioxide, hexanes: ethyl acetate 85:15) to provide 12.2 g of benzo[b]thiophene and 12.95 g (35% based on recovered starting material) of 3-(4-benzyloxyphenoxy)benzo[b]thiophene as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843965
Source datasetuspto-grants-1998_12
ORD IDord-8b34339e6d84415baaac7d41d327aee2
Source noteuspto-grants-1998_12