HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 178479105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | N-tert.-Butyl-N-(2-hydroxycyclohexyl)-hydrazine hydrochloride | HCID 14795576 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178479105 | HCID 178479105 | — |
Reaction Steps
A mixture of 13.35 g of N-tert.-butyl-N-(2-hydroxycyclohexyl)-hydrazine hydrochloride, 3.1 g of sodium cyanide and 50 ml of water is stirred in an ice bath and a 39% strength formalin solution (5.7 g) is added dropwise. The pH of the mixture is brought to 7 to 7.5 and the mixture is stirred at room temperature for 3 hours. The pH is then brought to 1 with concentrated hydrochloric acid and a solution of 6 g of sodium nitrite in 25 ml of water is added dropwise. After one hour, the nitroso compound is extracted with diethyl ether, the ethereal phase is dried and ethereal HCl is added. After 2 days, the precipitate is filtered off with suction and recrystallized from isopropanol/ethyl acetate. Yield: 4.5 g melting point: 174°-5° C. (decomp.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05006540 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-efdfb5fc9141422f92b8d9d82a883350 |
| Source note | uspto-grants-1991_04 |