HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65644Generated: October 29, 2026
Sodium Hydroxide → 8-Methylsulfonyl-12-hydroxy-5-heptadecynoic acid
https://huagongshe.com/reaction/65644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21317523 | HCID 21317523 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-Methylsulfonyl-12-hydroxy-5-heptadecynoic acid | HCID 21317627 | — |
Reaction Steps
Methyl 8-methylsulfonyl-12-acetoxy-5-heptadecynoate (41.6 g., 0.10 mole) is added to a solution of sodium hydroxide (12.0 g., 0.3 mole) in water (120 ml.) and methanol (600 ml.). The resulting solution is heated at 55°-60° C. for 24 hours. Most of the methanol is removed by evaporation in vacuo. The residue is diluted with water and extracted with ether. The aqueous solution is acidified with concentrated hydrochloric acid. The product which separates is taken up in ether, washed with water and dried over sodium sulfate. Evaporation of the ether in vacuo leaves the title compound as a viscous yellow oil. Purification is effected by column chromatography on silica gel with 2% methanol in chloroform as eluant. The title compound is obtained as a nearly colorless viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04128564 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-b6d62277561a48ee8102289c9f51c685 |
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| Source note | uspto-grants-1978_12 |
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