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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473776Generated: October 30, 2026

Water → HCID 58428106, compound

https://huagongshe.com/reaction/1473776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 58428193HCID 58428193—
SolventDichloromethaneHCID 6344—
ProductHCID 58428106HCID 58428106—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-hydroxy-8-methoxy-1-methoxymethoxy-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one (compound P2ii.6 obtained in analogy to preparation example 11, step 5) (500 mg, 1.33 mmol) in dichloromethane (10 ml) under argon atmosphere at 0° C. was added 3 {acute over (Å)} molecular sieves (0.5 g), followed by bromotrimethylsilane (1.72 ml, 2.03 g, 13.28 mmol) dropewise and the reaction mixture was stirred at 0° C. for one hour and at room temperature for 48 hours. The mixture was poured on cold water, the water layer saturated with sodium chloride and thoroughly extracted with dichloromethane. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (ethyl acetate). Yield: 40 mg of 1,4-dihydroxy-8-methoxy-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one (title compound P2ii.4) as a white solid, mp 152-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018135B2
Source datasetuspto-grants-2015_04
ORD IDord-bdb1d9bc56354935ae3ec0e3b1584b9b
Source noteuspto-grants-2015_04