HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355297Generated: October 30, 2026
Hydrochloric Acid → HCID 14874130, compound
https://huagongshe.com/reaction/355297
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | methyl (S)-3-fluorononanoate | HCID 54241495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14874130 | HCID 14874130 | 79.2% |
Reaction Steps
Under nitrogen atmosphere, 1 ml of dry tetrahydrofuran (THF) and 88 mg (2.3 mM) of lithium aluminum hydride were placed in a two-necked round-bottomed flask and cooled on an ice path. To the mixture, a solution of 400 mg (2.1 mM) of methyl (S)-3-fluorononanoate in 1 ml of dry THF was added dropwise. The ice bath was removed and the resultant mixture was stirred for 2 hours at room temperature. After the reaction, the reaction vessel (flask) was cooled on an ice bath. To the resultant reaction mixture, 0.5 ml of saturated sodium sulfate was added, followed by stirring for 30 minutes. To the resultant mixture, 4 ml of 3M-hydrochloric acid (HCl) was added, followed by extraction with Et2O. The organic layer was washed with 5 wt. %-sodium hydrogencarbonate aqueous solution and dried with anhydrous magnesium sulfate, followed by distilling-off of the solvent under reduced pressure to obtain 270 mg (1.66 mM) of (S)-3-fluorononanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05830386 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-1fbfc6996d364b3bb2eeb39ce2fb923c |
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| Source note | uspto-grants-1998_11 |
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