HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744688Generated: October 30, 2026
Hydrochloric Acid → HCID 131717786, compound
https://huagongshe.com/reaction/744688
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 19422061 | HCID 19422061 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131717786 | HCID 131717786 | — |
Reaction Steps
Serotonin hydrochloride hemihydrate (222 mg), N-(4-methoxyphenyl)-7-oxo-octanamide (263.3 mg), and methanol (10 mL) were stirred in the dark and the resulting solution treated with sodium cyanoborohydride (95 mg). After 4 d at ca. 22° C., sodium bicarbonate (350 mg) and water (10 mL) were added. After stirring 1.5 hours, the mixture was extracted with 1:4 2-propanol:dichloromethane (3×25 mL) and the combined extracts were dried (Na2SO4) and concentrated in vacuo. Chromatography eluting with 4:10:90, then 3:30:70 triethylamine:ethanol:ethyl acetate gave a component with an Rf of 0.3 in the latter solvent system. This oil was reconcentrated twice from ethanol (50 mL), then redissolved in ethanol (ca. 50 mL), treated with 1:9 concentrated hydrochloric acid:ethanol (1.2 mL), and reconcentrated in vacuo to a pale yellow oil which foamed to a solid. This was the title compound (352 mg), isolated as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559143 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-5522a96eeaad4f8eae0630f48c88df12 |
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| Source note | uspto-grants-1996_09 |
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