Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376991Generated: November 1, 2026

Sodium borohydride → HCID 11596162, compound

https://huagongshe.com/reaction/2376991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21099432HCID 21099432—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 11596162HCID 1159616288.2%

Reaction Steps

Sodium borohydride (89 mg, 1.8 mmol) was added to a solution of 2-({4-[(E)-2-(2,4-difluorophenyl)vinyl]phenyl}sulfonyl)benzaldehyde (Step 1; 233 mg, 0.61 mmol) in MeOH (7 mL) and CH2Cl2 (3 mL). After 2 h, the mixture was partitioned between CH2Cl2 (10 mL) and water (10 mL), the phases were separated and the aqueous portion extracted with further CH2Cl2 (10 mL). The combined organics were then dried (MgSO4), filtered and concentrated in vacuo. Purification by flash chromatography (eluant 40% EtOAc/isohexane) gave the title compound as a white solid (208 mg). δH (500 MHz, d6 DMSO): 8.08 (1H, d, J 7.7), 7.89-7.83 (5H, m), 7.77 (1H, d, J 7.6), 7.72 (1H, t, J 7.4), 7.55 (1H, t, J 7.5), 7.42-7.34 (2H, m), 7.33-7.27 (1H, m), 7.15 (1H, td, J 2.1, 8.4), 5.39 (1H, t, J 5.7), 4.69 (2H, d, J 5.7). m/z (ES+) 369 [(M-OH)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468393B2
Source datasetuspto-grants-2008_12
ORD IDord-34003f46b6da4803a59c1bf8633e0cf0
Source noteuspto-grants-2008_12