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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215183Generated: October 31, 2026

Hydrochloric Acid → tert-Butyl 2-[2-(2-aminoethyl)phenoxy]-2-methylpropionate

https://huagongshe.com/reaction/2215183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthylamineHCID 6341—
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyl 2-[2-(aminocarbonylmethyl)phenoxy]-2-methylpropionateHCID 21949727—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-[2-(2-aminoethyl)phenoxy]-2-methylpropionateHCID 21949731—

Reaction Conditions

Temperature50 °C

Reaction Steps

tert-Butyl 2-[2-(aminocarbonylmethyl)phenoxy]-2-methylpropionate (1.4 g, 4.87 mmol) was dissolved in tetrahydrofuran (5.0 mL). Subsequently, under nitrogen atmosphere, borane-THF complex in THF solution [1.0M BH3-THF in THF (14.6 mL, 14.6 mmol)] was added thereto, the mixture was stirred for three hours at 50° C. Thereafter, concentrated hydrochloric acid was gradually added thereto at 0° C. The resultant mixture was stirred for one hour at room temperature and made basic with an aqueous ethylamine solution. Ethyl acetate was added thereto. The mixture was sequentially washed with water and brine, followed by drying over sodium sulfate. The mixture was subjected to concentration under reduced pressure and purification by silica gel column chromatography (chloroform/methanol=30/1), whereby the target compound was obtained (830 mg, 2.97 mmol, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109226B2
Source datasetuspto-grants-2006_09
ORD IDord-c9d51f0e871f4e82a58c24330e18ba2e
Source noteuspto-grants-2006_09