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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870584Generated: October 26, 2026

Imidazole → (E)-3-[2(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acid

https://huagongshe.com/reaction/1870584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantLithium HydroxideHCID 3939—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantO-Coumaric AcidHCID 637540—
SolventDimethylformamideHCID 6228—
SolventOxolane--water (1/1)HCID 21881883—
Product(E)-3-[2(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acidHCID 2229046253.9%

Reaction Steps

To a solution of 8.2 g of (E)-3-(2-hydroxy-phenyl)-acrylic acid and 15.2 g of TBDMS-Cl in 10 ml of DMF was added 11.9 g of imidazole and the mixture was stirred at room temperature for 24 h. After aqueous work-up, the bis-silylated product was saponified with 2.1 g of LiOH in THF-H2O for 0.5 h at 0° C. The mixture was concentrated in vacuo and TBDMS-OH removed by extraction with hexane. The aqueous layer was acidified to pH 4 with KHSO4 and extracted with EtOAc. The organic phases were washed with brine, dried (Na2SO4) and evaporated to dryness. The semi-solid residue was suspended in hexane, filtered and the filtrate evaporated to dryness to yield 7.5 g of a pale yellow oil, which solidified upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096918
Source datasetuspto-grants-2000_08
ORD IDord-6705daeb889843aa95a7d9ee77323cb2
Source noteuspto-grants-2000_08