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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11215Generated: October 29, 2026

Hydrochloric Acid → HCID 21973123, compound

https://huagongshe.com/reaction/11215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Ethylenedioxy-1-phenylcyclohexanecarbonitrileHCID 69423715—
SolventTolueneHCID 1140—
ProductHCID 21973123HCID 2197312385%

Reaction Steps

At −78° C., 3-ethylenedioxy-1-phenylcyclohexanecarbonitrile (1.66 g, 6.83 mmol) in toluene (20 mL) was added DIBAL-H (1.0 M solution in toluene, 8.88 mL) slowly and was stirred for 1 hr. The reaction mixture was warmed up to room temperature and was added 1N HCl solution (2.60 mL) and was stirred for 1 hr. Saturated sodium bicarbonate was added to quench the reaction and the organic layer was separated. The aqueous layer was extracted with dichloromethane 3 times and the combined organic layers were dried over magnesium sulfate, filtered and concentrated under vacuum. The crude material was purified by filtering through a short silica gel pad with dichloromethane to give the title compound as a white sticky oil (1.43 g, 85% yield). 1H NMR (400 MHz, CDCl3) δ 1.32–1.40 (1H, m), 1.46–1.54 (1H, m), 1.72–1.86 (3H, m), 2.08 (1H, d, J=16 Hz), 2.59–2.67 (2H, m), 3.94–4.07 (4H, m), 7.15–7.36 (5H, m), 9.36 (1H, d, J=4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098203B2
Source datasetuspto-grants-2006_08
ORD IDord-11d6b4e2d7e343d0996c130ebd1192a0
Source noteuspto-grants-2006_08