HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → trans 3-Mercaptomethyl-2-oxo-1-azacyclodecane-10-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | trans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamide | HCID 86747204 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | trans 3-Mercaptomethyl-2-oxo-1-azacyclodecane-10-carboxamide | HCID 86747205 | — |
Reaction Steps
Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxamide (0.16 g, 0.56 mmol) is dissolved in ethanol (5.0 mL). An aqueous solution of 1N sodium hydroxide (0.60 mL, 0.60 mmol) is added, and the reaction is stirred for 1 hour. The reaction is acidified with 1N hydrochloric acid to a pH of about 3, and the solvent is evaporated. The residue is partitioned between ethyl acetate and water, and the aqueous layer is extracted several times with ethyl acetate. The combined organic layers are dried (Na2SO4), and the solvent is evaporated to give trans 3-mercaptomethyl-2-oxo-1-azacyclodecane-10-carboxamide, m.p. 185°-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05426103 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-f61d6cfb4770496da0610fe231ef78df |
| Source note | uspto-grants-1995_06 |