HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059072Generated: October 30, 2026
Sodium borohydride → HCID 11369630, compound
https://huagongshe.com/reaction/2059072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13345543 | HCID 13345543 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11369630 | HCID 11369630 | 82.4% |
Reaction Steps
10 grams of 6-n-propyl-8β-methoxycarbonylergoline were added to a mixture of 10 g of sodium borohydride in 125 ml of methanol. The reaction mixture was refluxed for about 2 hrs; then a second 5 g batch of sodium borohydride was added. The reaction mixture was cooled after 5 hrs, diluted with water, and the precipitate was filtered to give 7.5 g of 6-n-propyl-8β-hydroxymethylergoline melting at about 166°-168° C. A solution of 15 g of 4-toluenesulfonyl chloride in 100 ml of pyridine was added slowly to a cooled solution of 7.5 g of 6-n-propyl-8β-hydroxymethylergoline in 300 ml of pyridine. The mixture was stirred for 7 hrs whereafter it was poured over iced water and the precipitate was filtered to give 9 g of 6-n-propyl-8β-toxyloxymethylergoline melting at 147°-150° C.
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-a58082bc0e1340e4a5cb479645030216 |
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| Source note | uspto-grants-1982_03 |
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