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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715398Generated: November 3, 2026

Acetic Acid → 3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde oxime

https://huagongshe.com/reaction/1715398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehydeHCID 137329917—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde oximeHCID 137329919112.9%

Reaction Steps

3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde (12.7 g, 44.6 mmol) was dissolved in CH3CN (53 mL). To this sol. was added NaHCO3 (11.2 g, 134 mmol), and the mixture was stirred vigorously for 5 min. Water (96 mL) was added and the mixture was stirred for 10 min. NH2OH—HCl (6.20 g, 89.2 mmol) was added dropwise, followed by TBAC (622 mg, 2.24 mmol). The mixture was stirred at rt for 1 h, and AcOH (4.00 mL) was added dropwise to pH 6-7. The mixture was diluted with water (100 mL), and this mixture was extracted with Et2O (3×). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Drying the residue under high vacuum yielded the crude title compound (15.1 g, 98%) that was used further without purification. LC-MS: tR=1.09 min; ES+: 341.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799805B2
Source datasetuspto-grants-2010_09
ORD IDord-b74387f8727d4468881099a4baad25f8
Source noteuspto-grants-2010_09