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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255436Generated: November 3, 2026

HCID 19023661, compound → HCID 19023662, compound

https://huagongshe.com/reaction/2255436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19023661HCID 19023661—
ReactantHCID 70155070HCID 70155070—
SolventEthanolHCID 702—
ProductHCID 19023662HCID 1902366282.4%

Reaction Steps

To a stirred solution of 2-(3,4-dihydro-2H-1-benzopyran-4-yl]ethanal (2.50 g, 14.28 mmol) and 4-acetamidopiperidine AcOH (2.88 g, 14.28 mmol) (preparation described in U.S. Pat. No. 5,028,616) in ethanol (80 ml) under a nitrogen atmosphere, borane/pyridine complex (1.5 ml, 15 mmol) was added. The reaction mixture was stirred overnight (ca 15 h) and evaporated to an oily gum which was neutralized by careful addition of 10% hydrochloric acid. The acidic solution was extracted with diethyl ether and the diethyl ether extracts were discarded. The acidic aqueous layer was basified by dropwise addition of a 50% sodium hydroxide solution. The basic solution (>pH 12) was extracted with ethyl acetate. The ethyl acetate layer was washed with distilled water, dried (Na2SO4), filtered and evaporated to afford an oily gum (3.56 g). The resulting gum was purified by chromatography on silica (eluant: chloroform/ethanol/ammonium hydroxide; 85/14/1) to afford an oil (2.56 g) which was crystallized from diethyl ether to afford the title compound (2.40 g, 56%) mp=126-8°. Anal: C18H26N2O2Calc.: C 71.49; H 8.67; N 9.26; Found C 71.46; H 8.84; N 9.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240943
Source datasetuspto-grants-1993_08
ORD IDord-674ccddb174b4a7c8c5eb7e56a3b9031
Source noteuspto-grants-1993_08