HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429536Generated: October 27, 2026
Diisopropylamine → 1-(2-Benzyloxy-1-hydroxy-ethyl)-cyclohexanecarbonitrile
https://huagongshe.com/reaction/429536
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Cyanocyclohexane | HCID 69834 | — |
| Reactant | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Lithium diisopropylamide | HCID 2724682 | — |
| Product | 1-(2-Benzyloxy-1-hydroxy-ethyl)-cyclohexanecarbonitrile | HCID 18388337 | 73% |
Reaction Steps
Lithium diisopropylamide was prepared by dropwise addition of n-BuLi (2.03 mL; 2.5 M in Hexanes; 5.08 mmol) to a stirred and cooled (−10° C.) solution of i-Pr2NH (0.84 mL; 6.0 mmol) in dry tetrahydrofuran (40 mL). Stirring was continued for 20 minutes. The mixture was cooled to −78° C. and cyclohexane carbonitrile 1 (500 mg; 4.62 mmol) was added over 5 minutes. After a further 30 minutes, benzyloxyacetaldehyde (0.97 mL; 6.93 mmol) was added dropwise. Stirring was continued at −78° C. for 7 hours. The reaction mixture was then allowed to stir overnight at −20° C. Saturated aqueous NH4Cl was added (10 mL), and the mixture was extracted with diethyl ether (2×20° mL), dried over MgSO4 and evaporated. The residue was purified over silica gel chromatography (ether/heptane 1:1) to give 2 as a white solid (872 mg; 3.37 mmol; 73%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316638B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-434f85a4ccee406586eef21d65f7b1b3 |
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| Source note | uspto-grants-2001_11 |
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