HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380652Generated: October 29, 2026
Hydrochloric Acid → (1RS,2RS,3RS)-2-Carbomethoxy-3-hydroxy-tropane, hydrochloride
https://huagongshe.com/reaction/2380652
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (1RS,2RS)-2-Carbomethoxy-3-tropanone | HCID 131718787 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1RS,2RS,3RS)-2-Carbomethoxy-3-hydroxy-tropane, hydrochloride | HCID 131718788 | — |
Reaction Steps
To a solution of (1RS,2RS)-2-carbomethoxy-3-tropanone (17 g, 85 mmol) in 750 ml methanol cooled to -35° C. was added sodium borohydride (17 g, 450 mmol) and the mixture was stirred for 4 hours, The cooled solution was quenched by slow addition of concentrated hydrochloric acid (40 ml) and the mixture was concentrated in vacuo. Water (400 ml) was added and the pH was adjusted to 3 by addition of concentrated hydrochloric acid. After having washed the water phase three times with diethyl ether pH was adjusted to 11 by addition of concentrated ammonium hydroxide and the water phase was extracted three times with methylene chloride. Concentration in vacuo yields an oil which was dissolved in ethanol and added concentrated hydrochloric acid followed by concentration in vacuo. Freeze drying the residue yielded the title compound as an amorphous product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05369113 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-f49607ddf6cf4ff5b7ee0796fbab2d18 |
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| Source note | uspto-grants-1994_11 |
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