HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526257Generated: October 29, 2026
Hydrochloric Acid → HCID 117667437, compound
https://huagongshe.com/reaction/1526257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 89133951 | HCID 89133951 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 117667437 | HCID 117667437 | 94.5% |
Reaction Steps
Under a nitrogen atmosphere, to a mixture of (1R,2S)-2-(benzylamino)cyclopentanol (1.36 g), 1,2-dichloroethane (34 mL), and a 37% aqueous formaldehyde solution (1.73 mL) was added sodium triacetoxyborohydride (4.52 g), followed by stirring at room temperature overnight. To the reactant was added a saturated aqueous sodium hydrogen carbonate solution, and then acidified by the addition of 1 M hydrochloric acid. The aqueous phase was washed with ethyl acetate. The water phase was basified with a 1 M aqueous sodium hydroxide solution, and then chloroform was added thereto, followed by liquid separation. The organic phase was washed with saturated brine and dried over anhydrous magnesium sulfate. The mixture was filtered and then the filtrate was concentrated under reduced pressure to obtain (1R,2S)-2-[benzyl(methyl)amino]cyclopentanol (1.38 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085540B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-1ce045070f6f4f7daff4ff0352e2a979 |
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| Source note | uspto-grants-2015_07 |
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