HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanoacetic acid → n-(4-chlorobenzyl)-2-cyanoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | n-(4-chlorobenzyl)-2-cyanoacetamide | HCID 690673 | 89% |
Reaction Steps
According to the Scheme 1 Step 1: A mixture of 4-chlorobenzylamine (10.0 g, 71 mmol), cyanoacetic acid (6.13 g, 72 mmol), HOBt (11 g, 72 mmol), EDCI.HCl (20 g, 106 mmol) in 100 mL of dioxane was stirred for 3 h at room temperature. The solvent was removed under vacuum and 300 mL of DCM was added. The organic layer was successively washed with 2×100 mL of water, 2×50 mL of a solution 1N of NaOH, 4×100 mL of water until neutral pH. The organic layer was dried over Na2SO4, filtered and concentrated to afford N-(4-chlorobenzyl)-2-cyanoacetamide 1(A) (13.12 g, 89%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08779129B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-0725fff2b58f4b3f98b9f311e491f90d |
| Source note | uspto-grants-2014_07 |