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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375457Generated: November 2, 2026

Hydrochloric Acid → HCID 58638077, compound

https://huagongshe.com/reaction/2375457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
ReactantNitrogenHCID 947—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 23614741HCID 23614741—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 58638077HCID 58638077—

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of 109.4 g (349 mmol) 1-7 in 2.2 L of EtOH and 105 mL (1.05 moles) of 10 M NaOH in a 10 L round bottom was heated at 60° C. for 4 h, cooled to room temperature and aged overnight. To this mixture was added 90.2 mL (1.08 moles) of concentrated HCl and the solvents were removed by rotary evaporation. The residue was suspended in 2 L of acetonitrile and again taken to dryness by rotary evaporation. The solids were suspended in 3.8 L of CH2Cl2 and 200 mL of DMF, 118.7 g (1.75 moles) of imidazole was added, followed by 110.5 (733 mmol) of TBSCl. After stirring for 15 h under a gentle stream of N2, the reaction was dumped into 4 L of water and 2 L of CH2Cl2, the layers were separated, and the aqueous layer was extracted with 2 L of CH2Cl2. The combined organic extracts were then washed with 4×4 L of water, dried over Na2SO4, and concentrated by rotary evaporation. The residue was dissolved in 500 mL of MeOH and 500 mL of 2M MeNH2 in MeOH, stirred for 4 h, and then concentrated by rotary evaporation. The residue was placed under high vacuum until a constant weight was obtained, and the material was crushed with a mortar and pestle to provide 1-8 as a beige solid. Data for 1-8: 1HNMR (500 MHz, CDCl3) δ 7.6-7.3 (m, 5H), 7.1-6.9 (m, 3H), 6.75 (s, 1H), 4.25 (d, 1H), 4.1 (d, 1H), 3.95 (d, 1H), 3.75 (d, 1H), 0.9 (s, 9H), 0.1 (s, 3H), 0.05 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465746B2
Source datasetuspto-grants-2008_12
ORD IDord-97afe185d2364871952b22c951e52ece
Source noteuspto-grants-2008_12