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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425001Generated: October 27, 2026

Sodium hydride → HCID 67245854, compound

https://huagongshe.com/reaction/2425001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzenesulfonyl chloride, 3-(acetylamino)-4-methoxy-HCID 77351—
Reactant5-methoxy-3-methyl-1H-indoleHCID 11137444—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67245854HCID 67245854—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (2.15 grams, 49.3 mmol) was taken into a 250 mL three-necked round bottom flask containing tetrahydrofuran (50 mL) under nitrogen atmosphere. Added a solution of 5-methoxy-3-methyl indole solution (5.3 grams, 32.9 mmol) in tetrahydrofuran (25 mL) to the above mixture at 25° C., over a period of 15 minutes. The above reaction mass was stirred further for a period of 1 hour and mass was cooled to 0° C. and a solution of 3-acetamido-4-methoxy benzenesulfonyl chloride (13.01 grams, 49.3 mmol) in tetrahydrofuran (65 mL) was added through a dropping funnel over a period of 20 minutes. This mass was allowed to cool to room temperature and stirred over night (˜24 hours). The progress of the reaction was monitored by thin layer chromatography. After completion of the reaction it was quenched into ice water (100 mL) under stirring and extracted the product with ethylacetate (2×250 mL). Organic phase was washed with brine solution, dried over anhydrous sodium sulphate and concentrated under reduced pressure to obtain thick syrupy mass, which was used as such for the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964627B2
Source datasetuspto-grants-2011_06
ORD IDord-f4ff7d9f64fd4e748f60f00434b9bd04
Source noteuspto-grants-2011_06