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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387006Generated: October 30, 2026

Hydrochloric Acid → HCID 21182750, compound

https://huagongshe.com/reaction/1387006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
ReactantSodium ethanethiolateHCID 4459711—
ReactantHCID 10667130HCID 10667130—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductSodium ethanethiolateHCID 4459711—
ProductHCID 21182750HCID 2118275078%

Reaction Steps

A ˜0.5 M solution of sodium thioethoxide was prepared by adding ethanethiol (1.60 mL, 21.4 mmol) to a suspension of 60% NaH dispersion in mineral oil (769 mg, 19.2 mmol) in 40 mL of anhydrous DMF at 0° C. The ice bath was removed and the solution was stirred at room temperature for 30 min. The 0.5 M solution of sodium thioethoxide was then added dropwise to the solution of 4.00 g (10.7 mmol) of 2-(4-methoxyphenyl)benzo[b]thiophen-3-yl 4-methoxyphenyl ketone in 10.0 mL of anhydrous DMF at room temperature. The reaction mixture was heated at 85° C. for 3 h, then allowed to cool to room temperature, and acidified with 20 mL of 1.0 N HCl. To this was added 200 mL of H2O and the mixture was extracted with EtOAc (3×400 mL). The combined organic layers were washed with 200 mL of brine, dried over MgSO4, and concentrated under reduced pressure. The crude product was purified by PrepLC (30% EtOAc in hexanes) to afford 3.017 g of the title compound (8.37 mmol, 78%) as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-69bdad64d35f4670a95745f789492fc5
Source noteuspto-grants-2001_07