HuagongsheHuagongshe Chemistry Print Report · For research reference only
Gamma-Aminobutyric Acid → (4-Morpholinophenylsulphonylamino)butyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Morpholin-4-yl)benzene-1-sulfonyl chloride | HCID 14951211 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-Morpholinophenylsulphonylamino)butyric acid | HCID 19811002 | — |
Reaction Steps
10 g of 4-morpholinobenzenesulphonyl chloride is added to a solution comprising 3.94 g of 4-amino butyric acid and 4.6 g of sodium hydroxide in 80 cm3 of water, then 70 cm3 of tetrahydrofuran is added so as to obtain a solution. The temperature increases from 20° to 27° C. The solution is allowed to return to ambient temperature and maintained under agitation for 24 hours, after which it is acidified with acetic acid, and the solvent is evaporated under reduced pressure. The residue is taken up with 50 cm3 of distilled water; the precipitate is filtered off, washed with water, dried and 7.6 g of expected product is obtained, m.p.=163°-165° C., which is recrystallized from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05164514 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-c7d09ef79f4c437b980d8e7191d57d9d |
| Source note | uspto-grants-1992_11 |