HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75162Generated: October 28, 2026
HCID 68476611, compound → HCID 68477452, compound
https://huagongshe.com/reaction/75162
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68476611 | HCID 68476611 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68477452 | HCID 68477452 | 77.7% |
Reaction Steps
A stirred solution of N-((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)adamantane-1-carboxamide (3.07 g, 9.8 mmol) in dry THF (50 mL) was cooled in an ice bath and 1M BH3 in THF (50 mL, 50 mmol) was added. The ice bath was allowed to melt and the mixture was stirred over the weekend at rt. The mixture was poured into 5% aq HCl (50 mL). The mixture was concentrated on the rotary evaporator to leave a white solid which was taken up in 5% aq HCl (75 mL) and washed with ether (150 mL). The aqueous layer was made strongly basic by addition of NaOH and extracted with EtOAc (2×100 mL). The combined EtOAc extracts were dried over MgSO4 and concentrated to afford (1S,2R)-2-(1-adamantylmethylamino)-1-phenylpropan-1-ol (2.28 g, 77%) as an oil. LC-MS (3 min) tR=1.32 min, m/z=300.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835426B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-ab2a4e5d5da84c91aa65effef22d93d5 |
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| Source note | uspto-grants-2014_09 |
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