HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337232Generated: October 28, 2026
Hydrochloric Acid → HCID 71458420, compound
https://huagongshe.com/reaction/337232
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 71060086 | HCID 71060086 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 71458420 | HCID 71458420 | 10% |
Reaction Steps
[1-(4-Benzyloxycarbonylamino-benzyl)piperidin-4-yl]-carbamic acid tert-butyl ester (0.14 g, 0.32 mmol) was suspended in a 4M solution of HCl in Dioxane (5 ml). The resulting suspension was stirred at room temperature for 3 hours. After this time the solution was concentrated under vacuum and the resulting residue dissolved in THF (10 ml). To this solution was added diisopropylethylamine (0.28 ml, 1.6 mmol) was added in one portion, followed by the drop wise addition of acryloyl chloride (0.03 ml, 0.38 mmol) and the mixture was stirred at room temperature under a nitrogen atmosphere for 3 hours. After this time the mixture was diluted with DCM (20 ml) and washed sequentially with HCl (1M solution, 10 ml), NaOH (1M solution, 10 ml) and brine (10 ml). The organic layer was separated, dried (MgSO4), filtered, concentrated and the resulting residue was purified by flash column chromatography (elution: 100% DCM to 90% DCM, 10% Methanol) to give the title compound (0.012 g, 10% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889716B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-83479bbffa4d43438e60d10dc6c8d1c2 |
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| Source note | uspto-grants-2014_11 |
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