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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351643Generated: November 2, 2026

Sodium borohydride → HCID 21099499, compound

https://huagongshe.com/reaction/1351643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21099498HCID 21099498—
SolventEthanolHCID 702—
ProductHCID 21099499HCID 21099499133.4%

Reaction Steps

To a solution of 4-[(2-bromophenyl)thio]benzaldehyde (Step 1, 5 g, 12.7 mmol) in ethanol under nitrogen (63 mL) was added sodium borohydride (5.7 g, 127.2 mmol). The reaction was stirred at room temperature for 1 hour. The solvent was removed in vacuo and the residue partitioned between ethyl acetate and water. The organic layer was dried over Na2SO4 and the solvent removed in vacuo. The residue was purified by flash column chromatography on silica, eluting with 40% ethyl acetate/isohexane, to yield {4-[(2-bromophenyl)thio]phenyl}methanol as a colourless oil (5.0 g, 99%). δH (400 MHz, d6 DMSO): 7.65–7.60 (1H, m), 7.41 (4H, s), 7.27–7.21 (1H, m), 7.14–7.08 (1H, m), 6.83 (1H, dd, J=1.4, 7.9 Hz), 5.32–5.28 (1H, m), 4.56–4.53 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217740B2
Source datasetuspto-grants-2007_05
ORD IDord-8f4542e0bdf348939d6db0ba10d871af
Source noteuspto-grants-2007_05