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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206553Generated: October 31, 2026

Sodium hydride → HCID 117778922, compound

https://huagongshe.com/reaction/2206553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantIsovaleryl chlorideHCID 66054—
ReactantHCID 80156864HCID 80156864—
SolventDimethylformamideHCID 6228—
ProductHCID 117778922HCID 11777892248.89%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 2-methyl-1H-indole-3-carboxylate (300 mg, 1.30 mmol) in N,N-dimethylformamide (10 mL) was added sodium hydride (103.76 mg, 2.59 mmol, 60%). The mixture was stirred at 0° C. for 30 minutes. Then 3-methylbutanoyl chloride (234.60 mg, 1.95 mmol) was added at 0° C. and the mixture was stirred at room temperature (25° C.) for 2 hours. The mixture was cooled with ice, quenched with water (5 mL), diluted with ethyl acetate (20 mL), washed with brine (20 mL), extracted with ethyl acetate three times (20 mL×3), then dried over sodium sulfate. After concentration, the residue was purified by column on silica gel (0%-5% PE/EA) to afford the title compound (200 mg, yield: 48.89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-394f12e210344093adc8b439ca39ab77
Source noteuspto-grants-2016_06