HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360755Generated: November 2, 2026
Hydrochloric Acid → HCID 178443314, compound
https://huagongshe.com/reaction/2360755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-Mercaptopropionic Acid | HCID 6514 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 86652396 | HCID 86652396 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178443314 | HCID 178443314 | — |
Reaction Steps
3-Mercaptopropionic acid (150 mg, 1.41 mmol, 1.5 eq) can be added, under an atmosphere of dry nitrogen, to a stirred solution of sodium methoxide, prepared from sodium (64 mg, 2.78 mmol, 3 eq) and methanol (20 ml). After the initial white precipitate had dissolved, a solution of (3Z,6Z)-nona-3,6-dienyl p-toluenesulfonate (276 mg, 0.94 mmol) in diethyl ether can be added. The mixture can be stirred at 40° C. for several days under nitrogen, hydrochloric acid (10% v/v, 20 ml) and diethyl ether (20 ml) can be poured into the crude reaction mixture. The organic phase can be collected and washed with water and brine, and dried over sodium sulfate. The 3-(3E,6E)-nona-3,6-dienylthiopropionic acid produced can be dissolved in a solvent and PhSeBr and HgCl2 can added to the solution followed by an oxidizing agent to form a nitro-vinyl group at either on the 3-(3E,6E)-nona-3,6-dienylthiopropionic acid thereby producing, 3-(3E,6E)-6-nitronona-3,6-dienylthiopropionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686167B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-84caac542236469a837f392237cd10fd |
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| Source note | uspto-grants-2014_04 |
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