HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Chloride → 5-Chloro-1H-tetrazole-1-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Chloride | HCID 10477 | — |
| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Chloro-1H-tetrazole-1-acetic acid ethyl ester | HCID 12785792 | 78% |
Reaction Steps
A mixture of 130 g. (1 mole) of ethyl azidoacetate prepared as described in Part A and 96 g. (1.56 mole) of cyanogen chloride was heated at a temperature of 125° C. for 20 hours. After the reaction mixture had cooled, the reaction product mixture was dissolved in ethyl acetate, and the solution was filtered and evaporated in vacuo yielding a yellow crystalline mass of product. The yellow crystals were recrystallized from aqueous ethyl alcohol and gave 149 g. (78% yield) of ethyl 5-chloro-1H-tetrazol-1-ylacetate as pale yellow crystals melting at about 57°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04301282 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-a440f6e8985a49deb635c41abb1dfaf8 |
| Source note | uspto-grants-1981_11 |