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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810360Generated: November 1, 2026

Phenylpropanolamine → HCID 66607791, compound

https://huagongshe.com/reaction/1810360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylpropanolamineHCID 10297—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(2'-Formyl-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl)-acetic acid methyl esterHCID 86633167—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
SolventSodium BicarbonateHCID 516892—
ProductHCID 66607791HCID 66607791—

Reaction Steps

(2′-Formyl-6-methoxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid methyl ester (0.094 g, 0.27 mmol), (1R,2S)-(−)-norephedrine (0.054 g, 0.35 mmol), and sodium triacetoxyborohydride (0.113 g, 0.53 mmol) were combined in dichloroethane (1 mL). Acetic acid (1 drop) was added, and the reaction was stirred at room temperature for 40 minutes. Analytical tlc showed that only starting material was present, so the reaction was heated to 50° C. and stirred overnight. Analytical LCMS showed that some starting material was still present, so additional (1R,2S)-(−)-norephedrine (0.057 g, 0.38 mmol), and sodium triacetoxyborohydride (0.115 g, 0.53 mmol) were added, and the reaction was stirred for 3.5 hours at 50° C. After cooling to room temperature, the mixture was diluted with CH2Cl2 and saturated aqueous NaHCO3, and the aqueous layer was extracted twice with CH2Cl2. The combined organic layers were dried over MgSO4, filtered, and concentrated, and the residue was purified by silica gel chromatography (0-100% EtOAc in hexanes) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362044B2
Source datasetuspto-grants-2013_01
ORD IDord-ff730c5afff2493bb36bbe3e38ef5ab0
Source noteuspto-grants-2013_01