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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624156Generated: October 27, 2026

Sulfuric Acid → HCID 68750696, compound

https://huagongshe.com/reaction/624156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1,2-DibromoethaneHCID 7839—
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
Reactant4-Bromo-N,N-bis(trimethylsilyl)anilineHCID 4092620—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68750696HCID 68750696—

Reaction Steps

To a suspension of 2.2 g magnesium turnings (83.5 mmol) in 15 ml tetrahydrofuran were added 0.1 mL 1,2-dibromethane to start the Grignard reaction followed by slow addition of 13.0 g 2-(4-bromphenyl)-1,1,1,3,3,3-hexamethyldisilazane (41 mmol) in 70 mL tetrahydrofuran over a period of 20 minutes at room temperature with subsequent stirring for further 30 minutes. The resulting mixture was added dropwise at −78° C. to a solution of 4,5,6,7-tetrahydro-isobenzofuran-1,3-dione (5.6 g) in 70 mL tetrahydrofuran. The reaction mixture was slowly warmed to room temperature. Sulfuric acid (2 mL, 1 M) was added and the solvent was removed under reduced pressure. The residue was added carefully to 20 mL of 0.5 M sulfuric acid solution and the desired product started to precipitate and was extracted with ethyl acetate. Acidification of the water phase and extraction with ethyl acetate was continued until pH˜4-5 (at least three times). The combined organic phases were washed with brine, dried over magnesium sulfate, filtered and the solvent was subsequently evaporated under reduced pressure. Purification of the raw material by column chromatography with ethyl acetate/hexane 1:1 and subsequently 100% ethyl acetate resulted in the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302989B2
Source datasetuspto-grants-2016_04
ORD IDord-5ff8ed1be43f4f35b3959d63a2dd2232
Source noteuspto-grants-2016_04