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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242871Generated: October 30, 2026

Aniline → HCID 21939966, compound

https://huagongshe.com/reaction/1242871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantPivaloyl chlorideHCID 62493—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21939875HCID 21939875—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 21939966HCID 2193996641.9%

Reaction Steps

Triethylamine (0.11 ml) was added to THF suspension (3 ml) of 4-[[2-(2-piperidinoethyl)-6-tetralinyl]oxymethyl]benzoate (300 mg). Further, THF solution (0.5 ml) of trimethylacetyl chloride (92 mg) was added dropwise under ice-cooling, which was stirred for 30 minutes. The temperature of the reaction mixture was raised to room temperature, which was stirred for 1 hour. THF solution (0.5 ml) of aniline (85 mg) was added dropwise to the reaction mixture under ice-cooling, which was stirred for 1 hour. After the reaction mixture was stirred for 24 hours at room temperature, saturated sodium bicarbonate solution was added, and extraction was conducted using a mixed solution of ethyl acetate and THF. The organic layer was washed with water and saturated aqueous sodium chloride solution, dried, and then concentrated. The residue was recrystallized from THF-methanol-IPE to give the titled compound (150 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115750B1
Source datasetuspto-grants-2006_10
ORD IDord-01afb90724e245e39bf47801de9e4df6
Source noteuspto-grants-2006_10