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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294100Generated: November 3, 2026

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

https://huagongshe.com/reaction/2294100

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 numberUS05688800
Source datasetuspto-grants-1997_11
ORD IDord-bfc2ab97b99c4752a13b0f8a8bb83a79
Source noteuspto-grants-1997_11