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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937778Generated: October 31, 2026

Diethylether water → Ethyl 4-(4-cyano-3-hydroxyphenyl)butanoate

https://huagongshe.com/reaction/1937778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylether waterHCID 21584184—
ReactantEthyl 4-(4-cyano-3-t-butoxyphenyl)butanoateHCID 22461662—
SolventHydrochloric AcidHCID 313—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-(4-cyano-3-hydroxyphenyl)butanoateHCID 2246171182.1%

Reaction Steps

Ethyl 4-(4-cyano-3-t-butoxyphenyl)butanoate (6.8 g, 23.5 mmol) was dissolved in a mixture of acetonitrile (42 mL) and conc. HCl (3.85 mL) and allowed to stand for 80 min. The reaction was poured into ether/water and the ether layer separated. The ether layer was washed with water and brine, and the combined aqueous washes were reextracted once with ether. The combined ether layers were dried over sodium sulfate and concentrated to give 5.1 g of an off white waxy solid. This material was loaded onto a silica gel column (5×15 cm) in CHCl3 and eluted with 20% EtOAc in CHCl3 to yield 4.5 g of ethyl 4-(4-cyano-3-hydroxyphenyl)butanoate: 1H-NMR (CDCl3) 8.2 (1H, s), 7.42 (1H, d), 6.95 (1H, s), 6.77 (1H, d), 4.2 (2H, q), 2.63 (2H, dd), 2.39 (2H, dd), 1.96 (2H, m), 1.28 (3H, t); 13C (CDCl3) 174.4, 159.5, 149.2, 132.8, 120.8, 117.0, 116.1, 97.1, 60.9, 35.2, 33.6, 25.7. 14.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395919B1
Source datasetuspto-grants-2002_05
ORD IDord-2e952a669d914f9aa73ce36d19ef15e1
Source noteuspto-grants-2002_05