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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187446Generated: October 30, 2026

4-Phenylbutyric Acid → HCID 54165973, compound

https://huagongshe.com/reaction/2187446

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 numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-ca5cb7d7bb904e01a263d0a20e69e377
Source noteuspto-grants-2002_06