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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661550Generated: October 30, 2026

Sodium borohydride → HCID 17966951, compound

https://huagongshe.com/reaction/1661550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Formyl-2-(methylsulfanyl)benzonitrileHCID 17966635—
SolventMethanolHCID 887—
ProductHCID 17966951HCID 17966951—

Reaction Conditions

Temperature0 °C

Reaction Steps

A flask is charged with 5-formyl-2-methylsulfanyl-benzonitrile (1.0 g, 5.68 mmol) in MeOH (20 mL) and cooled to 0° C. Sodium borohydride (1.07 g, 28.40 mmol) is added and the mixture is stirred at room temperature for 2 h, followed by removal of solvent in vacuo. The residue is re-dissolved in dichloromethane and washed with water twice. The organic layer is dried over sodium sulfate and concentrated in vacuo to afford 5-hydroxymethyl-2-methylsulfanyl-benzonitrile as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 2.57 (s, 3H), 4.70 (d, J=5.1 Hz, 2H), 7.33 (d, J=8.3 Hz, 1H), 7.53 (dd, J=8.3, 1.0 Hz, 1H), 7.62 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-4a45c46170a6497794ee7fe88da52697
Source noteuspto-grants-2011_10