HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059073Generated: October 31, 2026
Sodium borohydride → HCID 70545904, compound
https://huagongshe.com/reaction/2059073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14380966 | HCID 14380966 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70545904 | HCID 70545904 | 89.3% |
Reaction Steps
8 grams of 6-isopropyl-8β-methoxycarbonylergoline was added to a mixture of 8 g of sodium borohydride in 200 ml of methanol. The reaction mixture was heated under reflux for 2 hrs; then a second 2 g batch of sodium borohydride was added. The mixture was cooled after 3 hrs, diluted with water, and the precipitate was filtered to give 6.5 g of 6-isopropyl-8β-hydroxymethylergoline, m.p. 192°-194° C., after crystallization from methanol. A solution of 13 g of 4-toluenesulfonyl chloride in 87 ml of pyridine was added slowly to a cooled solution of 6.5 g of 6-isopropyl-8β-hydroxymethylergoline in 250 ml of pyridine. After 15 hrs the mixture was poured over iced water and the precipitate was filtered to give 7.4 g of 6-isopropyl-8β-toxyloxymethylergoline melting at 180°-184° C. after crystallization from acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04321381 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-5e5a3e959a2c4ce5a9f7dd48dc137361 |
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| Source note | uspto-grants-1982_03 |
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