Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropyl chloroacetate | HCID 7759 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Naphthalenesulfinic acid | HCID 10888769 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 15027194 | HCID 15027194 | — |
Reaction Steps
44 g of 1-naphthalenesulfinic acid, 17.4 g of potassium carbonate, and 34.4 g of isopropyl chloroacetate were suspended in 45 ml of isopropyl alcohol. The suspension was then heated under reflux for 3 hours, after which the reaction mixture was cooled to 30° C. A 20% aqueous solution of 13.8 g of sodium hydroxide was added to the reaction mixture. The reaction system was then stirred for 1 hour. The resulting solution was diluted with 58 ml of water. 58 ml of 35% hydrochloric acid was then added to the reaction mixture. The resulting crystal was then filtered off, and air-dried. The yield was 54.9 g (95.8% of theoretical value).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05093229 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-69cd769e5b8e4bb4b979a5dc90fec02a |
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| Source note | uspto-grants-1992_03 |
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