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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75162Generated: October 28, 2026

HCID 68476611, compound → HCID 68477452, compound

https://huagongshe.com/reaction/75162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68476611HCID 68476611—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68477452HCID 6847745277.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835426B2
Source datasetuspto-grants-2014_09
ORD IDord-ab2a4e5d5da84c91aa65effef22d93d5
Source noteuspto-grants-2014_09