Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 178443989 | HCID 178443989 | — |
| Product | HCID 178476247 | HCID 178476247 | — |
Reaction Steps
100 ml of methanol, 80 ml of acetone and 2.9 ml of concentrated hydrochloric acid were added to 9.0 g (25.9 mmol) of N1-heptyl-N5- (1,1,3,3-tetramethylbutyl)-biguanide hydrochloride. The mixture was refluxed for 21 hours, and the solvent was distilled off under reduced pressure. To the residue were added 100 ml of ethanol, 60 ml of water and 10.6 ml of 5N sodium hydroxide, and the mixture was refluxed for 1 hour, concentrated under reduced pressure, and extracted with ethyl acetate. The extract was washed successively with 10% aqueous sodium acetate and water, and the solvent was distilled off under reduced pressure. The residue was recrystallized from methyl ethyl ketone two times to obtain 8.3 g of colorless crystals having a melting point of 98 to 101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622469B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-ca9f37f2bb284e78872987e8c4c335bf |
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| Source note | uspto-grants-2009_11 |
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