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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351676Generated: October 31, 2026

Sodium borohydride → HCID 11596162, compound

https://huagongshe.com/reaction/1351676

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, 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 numberUS07217740B2
Source datasetuspto-grants-2007_05
ORD IDord-d0364039da214877bb78e914653b5ec9
Source noteuspto-grants-2007_05