HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2428096Generated: October 31, 2026
Acetic Acid → 3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde oxime
https://huagongshe.com/reaction/2428096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde | HCID 137329917 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde oxime | HCID 137329919 | 112.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07968720B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-b90f016d63f74827a762e76ebeedacb9 |
|---|
| Source note | uspto-grants-2011_06 |
|---|