Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391286Generated: October 27, 2026

Ethanesulfonamide → HCID 49819974, compound

https://huagongshe.com/reaction/391286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonamideHCID 73702—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Ethoxy-4-(5-formylpyridin-3-yl)benzonitrileHCID 59578394—
CatalystTitanium isopropoxideHCID 11026—
SolventTolueneHCID 1140—
ProductHCID 49819974HCID 4981997472.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

Titanium(IV) isopropoxide (234 μL, 0.800 mmol) was added dropwise to a mixture of 2-ethoxy-4-(5-formylpyridin-3-yl)benzonitrile (101 mg, 0.400 mmol), ethanesulfonamide (52.4 mg, 0.480 mmol) in toluene (20 mL). The resulting mixture was heated at 140° C. for 2 hr. After concentration, the residue was dissolved in CH2Cl2 (10 mL) and sodium triacetoxyborohydride (254 mg, 1.200 mmol) was added at room temperature. The resulting mixture was stirred overnight, and quenched with NaHCO3 solution. After filtration, extraction and concentration, the residue was purified by flash column (MeOH—CH2Cl2, v/v, 1%-3.5%) and yielded a colorless oil (100 mg) which turned to colorless solid after standing. ESI-MS m/z: 317.9 [M+H]+, 1H NMR (400 MHz, CDCl3): δ 1.40 (t, J=7.4 Hz, 3H), 1.53 (t, J=7 Hz, 3H), 3.08 (q, J=7.4 Hz, 2H), 4.25 (q, J=7 Hz, 2H), 4.43 (d, J=6.2 Hz, 2H), 4.59 (brs, 1H), 7.10 (d, J=1.4 Hz, 1H), 7.19 (dd, J=8, 1.6 Hz, 1H), 7.66 (d, J=8 Hz, 1H), 7.93 (s, 1H), 8.62 (s, 1H), 8.77 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383827B2
Source datasetuspto-grants-2013_02
ORD IDord-7bbc0b061d314de69589128d45f2fb06
Source noteuspto-grants-2013_02