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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892817Generated: October 27, 2026

Hydrochloric Acid → tert-butyl 3-[(1S)-1-hydroxypropyl]benzoate

https://huagongshe.com/reaction/1892817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 3-formylbenzoateHCID 10845940—
Reactant(1S,2R)-(-)-2-(Dibutylamino)-1-phenyl-1-propanolHCID 11003877—
ReactantHCID 178418750HCID 178418750—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Producttert-butyl 3-[(1S)-1-hydroxypropyl]benzoateHCID 669348331,950.8%

Reaction Steps

To the (1S,2R)-2-di-n-butylamino-1-phenyl-1-propanol (200 mg) in toluene (7 ml) solution, tert-butyl 3-formylbenzoate (3 g) in hexane (7 ml) solution was added and the mixture was stirred at room temperature for 20 minutes. Next, diethylzinc in 1N hexane solution (33 ml) was added to the reaction solution under ice cooling and the mixture was stirred at that temperature for 18 hours. Saturated ammonium chloride aqueous solution was added to the reaction solution, the mixture was stirred at 20 minutes, and 1N hydrochloric acid was added. The obtained mixed solution was extracted with ethyl acetate. The organic layer was dried over with anhydrous sodium sulfate, then concentrated to obtain the title compound (3.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507714B2
Source datasetuspto-grants-2013_08
ORD IDord-1ae8f9d9b0f84ee3b80db555bfaf0f42
Source noteuspto-grants-2013_08