HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44345Generated: October 30, 2026
Heptanedinitrile → 2-Aminocyclohex-1-ene-1-carbonitrile
https://huagongshe.com/reaction/44345
Participants
| Role | Name | HCID | Charge |
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| Reactant | Heptanedinitrile | HCID 12590 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Aminocyclohex-1-ene-1-carbonitrile | HCID 290175 | 75% |
Reaction Steps
A stirred mixture of 1,7-heptanedinitrile (24.44 g, 0.2 mol) and t-BuOK (22.44 g, 0.2 mol) was heated at 80° C. for 3 h under nitrogen. The mixture was then cooled down to room temperature and stored at that temperature overnight. The residue was treated with water, and extracted with ether (2×). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by recrystallization from MeOH to give the title compound as a white solid (18.2 g, 75%). 1H NMR (400 MHz, CDCl3) δ1.58-1.71 (m, 4H), 2.12-2.20 (m, 4H), 4.23 (bs, 2H). MS 123 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541421B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-59996fd215b344649fc9a3bf2832919f |
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| Source note | uspto-grants-2013_09 |
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