HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11215Generated: October 29, 2026
Hydrochloric Acid → HCID 21973123, compound
https://huagongshe.com/reaction/11215
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Ethylenedioxy-1-phenylcyclohexanecarbonitrile | HCID 69423715 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21973123 | HCID 21973123 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098203B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-11d6b4e2d7e343d0996c130ebd1192a0 |
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| Source note | uspto-grants-2006_08 |
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