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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956492Generated: November 1, 2026

HCID 22860775, compound → HCID 10811257, compound

https://huagongshe.com/reaction/1956492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22860775HCID 22860775—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 10811257HCID 1081125770%

Reaction Steps

A solution of 3.6 g (7.27 mmol) of 4-benzyl-2-(S)-(3,5-bis(trifluoromethyl)benzyloxy)-3-(R)-phenylmorpholine in 100 mL of ethanol and 5 mL of water, containing 0.72 g of 10% Pd/C was hydrogenated on a Parr apparatus for 36 h. The catalyst was filtered and thoroughly washed with EtOAc. The filtrate was concentrated and the residue was partitioned between water and EtOAc. The EtOAc layer was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography using a gradient of 10-60% EtOAc/hexane to isolate 2.05 g (70%) of 2-(S)-(3,5-bis(trifluoromethyl)benzyloxy)-3-(R)-phenylmorpholine. 1H NMR (CDCl3) 1.92 (br s, 1H), 2.91 (m, 1H), 3.05 (td, J=11Hz and 3 Hz, 1H), 3.68 (d, J=7 Hz, 1H), 3.81 (td, J=11 Hz and 3 Hz, 1H), 4.01 (m, 1H), 4.44 (d, J=7 Hz), 4.5 (d, J=13 Hz, 1H), 4.85 (d, J=13 Hz, 1 H), 7.28-7.42 (m, 7H), 7.67 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780467
Source datasetuspto-grants-1998_07
ORD IDord-095c0484d04d46b3bc4ac82227ee947d
Source noteuspto-grants-1998_07