Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13433566 | HCID 13433566 | — |
Reaction Steps
0.85 g of 2-cyano-2-propanol and solution F were mixed and stirred for 15 minutes at 0° C. To the mixture was added 0.8 ml of chloroacetic chloride and the solution was stirred for 5 minutes at 0° C., additional 2 hours at room temperature and further 1 hour at 70° C. Then, to the reaction mixture was added 1N hydrochloric acid and water, and extracted with ethyl acetate. The organic layer was washed successively with water and aqueous solution of sodium bicarbonate, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue obtained was subjected to silica gel column chromatography to give 0.25 g of (1-cyano-1-methylethyl) chloroacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439266B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-ede42d2471de4f93832a2f69a3bbbc91 |
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| Source note | uspto-grants-2008_10 |
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