HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → Dicyclohexylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | HCID 178527651 | HCID 178527651 | — |
| Product | Dicyclohexylamine | HCID 7582 | — |
| Product | HCID 178527651 | HCID 178527651 | — |
Reaction Steps
A mixture of 21.5 g. (0.087 mol.) of methyl 2-sulfoethyldithiocarbamate potassium salt (0.5 hydrate) and 7.16 g. (0.11 mol.) of sodium azide in 200 ml. of water was refluxed for 2 hours. The solution was cooled to 25° and extracted with ethyl acetate. The aqueous phase was treated with Amberlite IR-120H resin, washed with ether and evaporated to give an oil. The oil was dissolved in acetone, the solution was filtered and the filtrate was evaporated to dryness to give 1-(2-sulfoethyl)-tetrazole-5-thiol. The thiol was dissolved in isopropanol, cyclohexylamine was added until pH 8-9 and acetonitrile was added to give 1-(2-sulfoethyl)tetrazole-5-thiol as the di-cyclohexylamine salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118490 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-b6a55b080b5441ddb9e3012462b1c05a |
| Source note | uspto-grants-1978_10 |