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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954812Generated: November 3, 2026

4-Phenylbutyric Acid → HCID 54165973, compound

https://huagongshe.com/reaction/1954812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenylbutyric AcidHCID 4775—
ReactantTriethylamineHCID 8471—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
ProductHCID 54165973HCID 54165973—

Reaction Steps

4-Phenylbutyric acid (1.0 g, 6.1 mmol) was dissolved in thionyl chloride (15 mL) and heated at reflux for 1 h. The excess of thionyl chloride was evaporated in vacuo, the residue was treated with toluene and again the solvent was removed in vacuo. Crude acid chloride (86 mg, 0.47 mmol) was dissolved in methylene chloride (5 mL) and added dropwise to an ice-cooled solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (110 mg, 0.45 mmol) and triethylamine (93 μL, 0.68 mmol) in methylene chloride (15 mL). After the addition, the reaction was allowed to stir at ambient temperature for 15 min and was then washed with water. The phases were separated and the organic phase was dried (Na2SO4), filtered and evaporated in vacuo to give a crude product which was purified on a silica gel column using chloroform/ethanol saturated with NH3 (100:4) as the eluent. Yield: 150 mg (82%) of the title compound as white crystals: mp 137-139° C.; [α]21D+8.4° (c 0.50, chloroform); EIMS (70 eV) m/z (relative intensity) 391 (23, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124283
Source datasetuspto-grants-2000_09
ORD IDord-1f47e472006640fdb62ade29b2e37b26
Source noteuspto-grants-2000_09