HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (R)-(+)-4-tert. Butoxy-2-methylbutyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | (S)-(+)-3-tert. butoxy-2-methyl-1-propyl p-toluenesulfonate | HCID 86735106 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-(+)-4-tert. Butoxy-2-methylbutyronitrile | HCID 86735109 | — |
Reaction Steps
A mixture of 6.4 g. (0.021 mole) of (S)-(+)-3-tert. butoxy-2-methyl-1-propyl p-toluenesulfonate and 2.09 g. (0.043 mole) of sodium cyanide in 63 ml. of ethanol and 7 ml. of water was stirred and refluxed for 11 hours. After cooling, the reaction mixture was diluted with ice-water and worked up by extraction with CH2Cl2 in the manner of Example 1. The crude product (3.7 g.) was chromatographed on 125 g. of silica gel. Elution with 4:1 parts by volume hexane-ether gave 2.98 g. (91.7%) of R-(+)-4-tert.-butoxy-3-methylbutyronitrile as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04051153 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-964a2da25eb34e33a1ecc4a234c0707b |
| Source note | uspto-grants-1977_09 |