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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613131Generated: November 2, 2026

4-Chlorobutanoic acid → HCID 19775183, compound

https://huagongshe.com/reaction/1613131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutanoic acidHCID 12300—
Reactant1,2,3,4-Tetrahydro-1-naphthylamineHCID 18066—
ReactantSodium hydrideHCID 24758—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantButanamide, 4-chloro-N-(1,2,3,4-tetrahydro-1-naphthalenyl)-HCID 11265230—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 19775183HCID 1977518350.2%

Reaction Steps

CDI (6.61 g. 40.75 mmoles) and, after 1 hour, 1,2,3,4-tetrahydro-1-naphtylamine (5 g, 33.96 mmoles) were added to 4-chlorobutyric acid (4.16 g, 33.96 mmoles) in CH2Cl2 (200 mL) under stirring. The resulting solution was kept at room temperature for 40 hours, then washed with 1N HCl, NaHCO3 (saturated solution), H2O, NaCl (saturated solution) and dried over anhydrous Na2SO4. The solvent was evaporated and the residue taken up with CHCl3. Upon addition of Et2O under stirring a precipitate was obtained consisting of 4.5 g (17.87 mmoles) of N-(4-chloro-butyroyl)-1,2,3,4,-tetrahydro-1-naphtylamine (silica gel TLC; Eluant EtOAc-Hexane (1:1), RF=0.7) which was dissolved in CH3CN (100 mL). To the mixture, 80% NaH in mineral oil (804 mg, 26.8 mmoles) was added in two portions, the second portion after some hours following the first one. The mixture was then kept at room temperature under stirring for 2 days. The mixture was then filtered, the filtrate evaporated and the residue chromatographed on silica gel using EtOAc-Hexane (1:1) as eluant. 1.93 g of the title compound were obtained. Last step yield=50%, overall yield 26%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192759
Source datasetuspto-grants-1993_03
ORD IDord-108fd700b29a4d3bb2d0f99e1f5b9f72
Source noteuspto-grants-1993_03