HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492421Generated: October 29, 2026
HCID 131718785, compound → Hydrochloric Acid
https://huagongshe.com/reaction/1492421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 131718785 | HCID 131718785 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 86583652 | HCID 86583652 | — |
Reaction Steps
(1R,2R,3S)-2-Carbomethoxy-3-benzoxytropane, hydrochloride (100 g, 0.29 mol) was refluxed in 1000 ml 1M hydrochloric acid for 18 hours and the solution was ice cooled. Benzoic acid was collected by filtration and the filtrate was concentrated in vacuo. Trituration of the remanescens with ethanol and filtration yields (1R,2R,3S)-3-hydroxy-tropane 2 carboxylate, hydrochloride as a white crystalline compound which without further purification was dried and refluxed in phosphorous oxychloride (50 ml) for two hours. The solution was concentrated in vacuo and absolute methanol (150 ml) was slowly added under ice cooling. The solution was stirred at ambient temperature for 16 hours and was concentrated in vacuo. The remanescens was ice cooled and made basic by addition of a sodium hydroxide solution (10M, approximately 100 ml) and was extracted 5 times with diethyl ether. The combined organic phase was dried and concentrated in vacuo yielding an oil, which was distilled in vacuo (70°-74° C., 1 mBar) yielding the title compound as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05374636 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-d968f2e56820463a89c7279b37d29bd1 |
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| Source note | uspto-grants-1994_12 |
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