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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742309Generated: October 31, 2026

Ammonium Chloride → tert-Butyl 4-(1-hydroxypropyl)benzoate

https://huagongshe.com/reaction/742309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 4-formylbenzoateHCID 2751588—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl 4-(1-hydroxypropyl)benzoateHCID 21473763—

Reaction Steps

t-Butyl p-formylbenzoate (20 g, 97 mmol) was dissolved in ether (300 ml), followed by the dropwise addition of ethylmagnesium bromide (3M ethereal solution, 33 ml) under cooling with ice. The obtained mixture was stirred to complete a reaction. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride and the obtained mixture was extracted with ether. The organic phase was distilled to remove the solvent and the obtained residue was subjected to silica gel column chromatography and eluted with a solvent (ethyl acetate/hexane=1:4) to give 22.3 g of t-butyl 4-(1-hydroxypropyl)benzoate. This product was dissolved in petroleum ether (500 ml), followed by the addition of active manganese dioxide (165 g). The obtained mixture was heated under reflux for 30 hours to complete a reaction. The reaction mixture was filtered and the filtrate was concentrated to give 21.1 g of t-butyl 4-propionylbenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554615
Source datasetuspto-grants-1996_09
ORD IDord-0510194de25a419da8e567c741c45216
Source noteuspto-grants-1996_09