HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345359Generated: October 27, 2026
Hydrochloric Acid → HCID 86743789, compound
https://huagongshe.com/reaction/345359
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | KOtBu THF | HCID 66863523 | — |
| Reactant | HCID 86743787 | HCID 86743787 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86743789 | HCID 86743789 | — |
Reaction Steps
To 0.4 g of trans 1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-acetaldehyde in 5 ml anhydrous tetrahydrofuran under nitrogen, cooled to -78°, is added dropwise a solution of 1.17 g of methoxymethyl-triphenylphosphonium chloride in 15 ml of anhydrous tetrahydrofuran to which is added 1.55 ml of potassium tert-butoxide/tetrahydrofuran (1.6M). Solution is stirred at room temperature for 4 hours. 2N Hydrochloric acid (11 ml) is added and the mixture is stirred for 45 minutes. The solution is concentrated and then extracted with methylene chloride. The extract is dried over sodium sulfate, filtered, concentrated, and the residue is purified by flash chromatography using ethyl acetate/hexane (1:5 to 3:7) to yield trans 1-ethoxycarbonyl-2-ethoxycarbonylpyrrolidine-3-propionaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057506 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-d5c2e7d8a4204c229a4f33c275520fec |
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| Source note | uspto-grants-1991_10 |
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