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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721722Generated: October 30, 2026

HCID 22860715, compound → HCID 9909972, compound

https://huagongshe.com/reaction/1721722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22860715HCID 22860715—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 9909972HCID 990997264%

Reaction Steps

A solution of 115 mg (0.25 mmol) of the 2-(R)-(3,5-bis(trifluoromethyl)benzyloxy)-3-(R)-phenyl-4-(2-propenyl)-6-(R)-methyl morpholine (from Example 23, Step A) and 230 mg (0.25 mmol) of tris(triphenylphosphine)rhodium chloride in 15 mL of 4:1 v/v acetonitrile/water was heated at reflux for 30 min. The reaction was cooled and partitioned between 50 mL of ethyl acetate and 15 mL of water. The layers were separated and the organic layer was dried over magnesium sulfate. The aqueous layer was extracted with 2×25 mL of ethyl acetate; the extracts were dried and combined with the original organic layer. The combined organics were concentrated in vacuo. The residue was filtered through a pad of silica gel (~20 g) using 2:1 v/v ether/hexanes as the solvent. The filtrate was concentrated; flash chromatography on 5 g of silica gel using 17:3 v/v hexanes/ether as the eluant afforded 67 mg (64%) of 2-(R)-(3,5-bis(trifluoromethyl)benzyloxy)-3-(R)-phenyl-6-(R)-methyl morpholine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512570
Source datasetuspto-grants-1996_04
ORD IDord-f6f7b2d67d694fbd9c64c8a5d8cf085b
Source noteuspto-grants-1996_04