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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004094Generated: October 30, 2026

HCID 22860775, compound → HCID 10811257, compound

https://huagongshe.com/reaction/1004094

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=11 Hz 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 numberUS06048859
Source datasetuspto-grants-2000_04
ORD IDord-9d821f6264f74e5e99b39f650ffca210
Source noteuspto-grants-2000_04