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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736918Generated: October 27, 2026

Hydrochloric Acid → HCID 22184582, compound

https://huagongshe.com/reaction/736918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium borohydrideHCID 4311764—
Reactant4-amino-3-chloro-5-(trifluoromethyl)benzoic AcidHCID 4643549—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22184582HCID 2218458233.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

69.56 g (0.43 mol) CDI were added to a solution of 93.4 g (0.39 mol) 4-amino-3-chloro-5-trifluoromethyl-benzoic acid (described in Arzneim.-Forsch. 1984, 34(11A), 1612-1624) in 1 L THF and the mixture was stirred for 1 h at 40° C. The reaction mixture was then carefully added to a solution of 51.4 g (1.36 mol) NaBH4 in 450 mL of water at RT under a nitrogen atmosphere and with cooling. The mixture was stirred for 2 h at RT, combined with 500 mL water and 300 mL semiconc. HCl, stirred for another hour and then exhaustively extracted with EtOAc. The combined org. phases were dried over Na2SO4 and evaporated down i. vac. The oil remaining was combined with 500 mL PE and stirred while cooling with ice. The precipitate was suction filtered, washed with PE and dried. 29.7 g of the desired product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595312B2
Source datasetuspto-grants-2009_09
ORD IDord-88b81ef181254587abfa2ba7977e3706
Source noteuspto-grants-2009_09