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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473774Generated: October 30, 2026

Bromotrimethylsilane → HCID 58427991, compound

https://huagongshe.com/reaction/1473774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 58428041HCID 58428041—
SolventDichloromethaneHCID 6344—
ProductHCID 58427991HCID 58427991—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of carbonic acid ethyl ester 8-methoxy-1-methoxymethoxy-2-oxo-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-4-yl ester (compound P1 ii.7 obtained in analogy to preparation example 11, step 6) (1.0 g, 2.23 mmol) in bromotrimethylsilane (4.33 ml, 5.12 g, 33.44 mmol) under argon atmosphere was added 3 {acute over (Å)} molecular sieves (0.5 g) and the reaction mixture was stirred at 75° C. overnight. The mixture was diluted with dichloromethane, filtered, the filtrate evaporated, the residue triturated with cold diethyl ether, filtered and dried. The crude product was purified by chromatography on silica gel (gradient dichloromethane→dichloromethane/methanol 20:1→10:1). Yield: 580 mg of carbonic acid ethyl ester 1-hydroxy-8-methoxy-2-oxo-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-4-yl ester (compound P1ii.11) as a white solid, mp 154-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018135B2
Source datasetuspto-grants-2015_04
ORD IDord-a04a2f2af17e4138ad27aabe794c20ef
Source noteuspto-grants-2015_04