HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427466Generated: November 1, 2026
Hydrochloric Acid → 1-Cyanomethyl-cyclohexanecarboxylic acid methyl ester
https://huagongshe.com/reaction/2427466
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Methyl cyclohexanecarboxylate | HCID 20748 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Cyanomethyl-cyclohexanecarboxylic acid methyl ester | HCID 57657808 | 41% |
Reaction Steps
Treat a −78° C. solution of methyl cyclohexane carboxylate (15.0 g, 0.105 mol) in THF (150 mL) with a 2M solution of lithium diisopropylamide in heptane/THF/ethylbenzene (63.3 mL, 0.126 mol) and stir at −78° C. for 20 minutes under N2. Treat the reaction with bromoacetonitrile (25.31 g, 0.211 mol) and stir at −78° C. for 15 minutes. Warm the reaction to room temperature and stir 4 hours. Acidify the reaction with 1 N HCl and then dilute the reaction with ethyl acetate and wash with water. Dry the organic layer (Na2SO4) and remove the solvent in vacuo to afford crude product. Purify with a 0 to 30% ethyl acetate in hexanes gradient on silica gel to afford 7.78 g (41%) of the titled product. Rf=0.32 (3/1 hexanes/ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07968585B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-fa5e979fc0fc468c9726504a37d7b17b |
|---|
| Source note | uspto-grants-2011_06 |
|---|