HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973352Generated: October 29, 2026
Water → Ethyl 8-carbamoyl-12-hydroxy-12-methylheptadecanoate
https://huagongshe.com/reaction/973352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 8-carbamoyl-12-methyl-11-heptadecenoate | HCID 54022520 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Ethyl 8-carbamoyl-12-hydroxy-12-methylheptadecanoate | HCID 21401727 | — |
Reaction Steps
Mercuric acetate (3.8 g., 0.012 mole) is dissolved in water (12 ml.) and tetrahydrofuran (20 ml.) is added to give a suspension of a yellow solid. Then, ethyl 8-carbamoyl-12-methyl-11-heptadecenoate (4.2 g., 0.012 mole) in tetrahydrofuran (20 ml.) is added, and the mixture stirred at room temperature for 24 hours. After 6 hours, the yellow suspended solid has disappeared and a cloudy solution results. To the solution is added 3M sodium hydroxide solution (12 ml.), followed by 0.5M sodium borohydride solution in 3M sodium hydroxide (12 ml.). Liquids are decanted from the precipitated mercury. The organic layer is taken up in ether, washed with three portions of water and dried over sodium sulfate. Evaporation of the ether leaves 4.0 g. of ethyl 8-carbamoyl-12-hydroxy-12-methylheptadecanoate which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04055597 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-4c48f6c845524826a2bfa2016191cb3b |
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| Source note | uspto-grants-1977_10 |
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