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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 4-formylbenzoate | HCID 2751588 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-Butyl 4-(1-hydroxypropyl)benzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05554615 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-0510194de25a419da8e567c741c45216 |
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| Source note | uspto-grants-1996_09 |
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