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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892818Generated: October 31, 2026

Ammonium Chloride → tert-butyl 4-(1-aminopropyl)benzoate Hydrochloride

https://huagongshe.com/reaction/1892818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 4-formylbenzoateHCID 2751588—
ReactantAzane;hydrateHCID 12896473—
ReactantHCID 178418443HCID 178418443—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
Producttert-butyl 4-(1-aminopropyl)benzoate HydrochlorideHCID 66935393—

Reaction Steps

To copper (I) iodide (3.1 g) in diethylether (70 ml) suspension, ethylmagnesium bromide (0.89M tetrahydrofuran solution) (35 ml) was added at −23° C. and the mixture was stirred at that temperature for 20 minutes. Next, tert-butyl 4-formylbenzoate (3 g) in diethylether (10 ml) solution was added to the reaction solution and the mixture was stirred at −23° C. for 30 minutes. Saturated ammonium chloride aqueous solution and 28% ammonia water were added to the reaction solution, the mixture was stirred at room temperature for 40 minutes, and the mixture was extracted with ethyl acetate. The organic layer was successively washed with distilled water and saturated saline, dried over with anhydrous sodium sulfate, then concentrated. The obtained compound (3.7 g) was used as an starting material instead of the starting material of Reference Example 83, that is, the compound S82, while 4N hydrochloric acid/ethyl acetate was used instead of L-tartaric acid for the similar procedure as in Reference Example 83 to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507714B2
Source datasetuspto-grants-2013_08
ORD IDord-527e3fa9b4c448b4bf5c2db92ab00a22
Source noteuspto-grants-2013_08