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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 932169Generated: October 31, 2026

Tetrahydrofuran → HCID 68000480, compound

https://huagongshe.com/reaction/932169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantSodium ChloriteHCID 23668197—
Reactant2-((3R,5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxo-1-((1S)-1-(tetrahydro-2H-pyran-2-yl)propyl)piperidin-3-yl)acetaldehydeHCID 86660734—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Solvent2-Methyl-2-buteneHCID 10553—
ProductHCID 68000480HCID 68000480—

Reaction Steps

A solution of 2-((3R,5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-2-oxo-1-((1S)-1-(tetrahydro-2H-pyran-2-yl)propyl)piperidin-3-yl)acetaldehyde (3 mg, 5.97 μmoL; mixture of stereoisomers, Example 224, Step E) in a solution of 1.25 M potassium phosphate monobasic in water (0.050 mL), t-butanol (0.050 mL) and 2.0 M 2-methylbut-2-ene in THF (0.15 mL, 0.30 mmol) was treated with sodium chlorite (2.16 mg, 0.024 mmol) at ambient temperature for 3 h. The reaction was quenched with 1 M sodium thiosulphate solution (0.03 mL). After 10 min, the mixture was acidified with 1M potassium bisulphate solution (0.03 mL) and extracted with ethyl acetate. The organic layers were washed with sat. aq. NaCl solution and dried over anhydrous sodium sulfate. Purification by reversed phase preparatory HPLC (eluent: 0 to 100% MeCN +0.1% TFA in water +0.1% TFA, over 20 minutes) gave the title compound as the first eluting isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296736B2
Source datasetuspto-grants-2016_03
ORD IDord-8c8eab37a8534a979025b8cf52662aa6
Source noteuspto-grants-2016_03