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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114807Generated: October 31, 2026

Chlorotrimethylsilane → HCID 10535797, compound

https://huagongshe.com/reaction/2114807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3,5-Dihydroxybenzoic AcidHCID 7424—
ReactantAllyl AlcoholHCID 7858—
ProductHCID 10535797HCID 10535797—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To 1.5 g of 3,5-dihydroxybenzoic acid in screw-capped vial was added 10 g of allyl alcohol and the vial was closed and cooled to −20° C. To the cold contents of the reaction vial was added 5 mL of trimethylsilyl chloride via syringe through a septum. The reaction vial was allowed to warm to room temperature and agitated for 16 hours. The vial was opened carefully and its contents transferred to a round-bottomed flask. The solvent was removed under reduced pressure and the residual solid was dried under reduced pressure over potassium hydroxide pellets for 12 h. The semisolid product was used in the subsequent synthetic steps without further purification. The product was analyzed by HPLC and had a retention time of 3.65 on 5 cm C18 reversed phase column with flow rate of 2.5 mL/min of pure acetonitrile (for solvent A) and 0.1% aqueous trifluroacetic acid (for solvent B). The product was characterized by 1H NMR (DMSO-d6, 350 MHz): δ=6.87 (s, 2H, aromatic); 6.44 (s, 1H, aromatic); 5.85-5.96 (m, 1H); 5.16-5.33 (m, 2H); 4.65-4.67(dd, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435747B2
Source datasetuspto-grants-2008_10
ORD IDord-852180b23caa436d9547cead8fa59a70
Source noteuspto-grants-2008_10