HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280795Generated: October 30, 2026
Methanol → 4-Aminobicyclo[2.2.1]heptan-1-ol hydrochloride
https://huagongshe.com/reaction/2280795
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | benzyl N-{4-hydroxybicyclo[2.2.1]heptan-1-yl}carbamate | HCID 70981216 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Aminobicyclo[2.2.1]heptan-1-ol hydrochloride | HCID 86676355 | 97% |
Reaction Steps
A 2-L Parr bottle was charged with benzyl 4-hydroxybicyclo[2.2.1]heptan-1-ylcarbamate (61 g, 233 mmol), methanol (400 mL), and water (200 mL). The Parr bottle was flushed with nitrogen and charged with 10% palladium on carbon (25 g, 11.65 mmol, 50% wet with water). The reaction was run under 30 gpsi hydrogen on a parr shaker for 3 h when TLC analysis (15% methanol/DCM with 2% ammonium hydroxide) indicated a complete reaction. The reaction was filtered through a celite plug and concentrated to remove methanol. The resulting aqueous mixture was treated with 2 N hydrochloric acid (115 mL) until it reached pH 1-2. The aqueous mixture was extracted using ethyl acetate (5×400 mL) to remove an impurity. The aqueous mixture was concentrated to dryness and dried in a vacuum oven at 40° C. overnight to provide 36.91 g (97%) of 4-aminobicyclo[2.2.1]heptan-1-ol hydrochloride; MS (ESI) m/z 128.1 [M+1]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139534B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-75d89ddf03894c8ab8de90b029b179cd |
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| Source note | uspto-grants-2015_09 |
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