HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723027Generated: October 30, 2026
Ammonia → Ergoline-8-methanol, 2-bromo-9,10-didehydro-6-methyl-, (8beta)-
https://huagongshe.com/reaction/1723027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lysergol | HCID 14987 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | HCID 86743321 | HCID 86743321 | — |
| Product | Ergoline-8-methanol, 2-bromo-9,10-didehydro-6-methyl-, (8beta)- | HCID 181032 | — |
Reaction Steps
Dry gaseous hydrogen bromide is introduced into 100 ml of anhydrous dimethylsulfoxide at room temperature. The quantity of the introduced hydrogen bromide gas is measured by titrating with 0.1N sodium hydroxide solution. The hydrogen bromide is introduced until the concentration of the gas reaches 0.0003-0.0005 mole/ml. One g (0.003937 mole) of lysergol is dissolved in an aliquot amount of this hydrogen bromide-dimethylsulfoxide mixture which contains 12 equivalents of hydrogen bromide. After complete dissolution, this mixture is stirred at room temperature for 20 minutes, then poured into a 5-fold volume of ice-water. Thereafter, the solution is made alkaline by adding aqueous ammonia up to a pH value of 8.9, the precipitate is filtered off, washed with water, dried and purified on a Kieselgel column by using an 8:2 mixture of chloroform and methanol to give the named compound in a yield of 0.76 g (0.00228 mole, 58%), m.p.: 193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04859682 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-7c40ca1910e946b4ba0b0e83acfaf28b |
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| Source note | uspto-grants-1989_08 |
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