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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441797Generated: October 29, 2026

(p-Chlorophenyl)trmethylsilane → HCID 21417831, compound

https://huagongshe.com/reaction/441797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(p-Chlorophenyl)trmethylsilaneHCID 66351—
Reactant2-(methylamino)benzaldehydeHCID 267569—
ReactantMagnesiumHCID 5462224—
ReactantHCID 21417831HCID 21417831—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 21417831HCID 21417831—
ProductHCID 21417851HCID 21417851—

Reaction Steps

4-Methylamino-4'-trimethylsilylbenzhydrol was prepared by a Grignard reagent formulated from 0.2 mole of 4-trimethylsilylchlorobenzene and 0.2 mole of magnesium with 0.2 mole of N-methylaminobenzaldehyde. 0.4 mole of the thus obtained 4-methylamino-4'-trimethylsilylbenzhydrol was dissolved in pyridine, and to the resultant solution was added, dropwise over a period of 40 hours at room temperature, an oxidizing agent prepared by adding 125 ml of pyridine to a solution of 7.5 ml of water and 12.5 mole of chromic anhydride under agitation while being cooled with water. The reaction product was refined by chromatography using silica gel, to obtain 41 g of 4-methylamino-4'-trimethylsilyl benzophenone in a yield of 38%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04042613
Source datasetuspto-grants-1977_08
ORD IDord-ec764d0c43b74074811fa9878085baf4
Source noteuspto-grants-1977_08