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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725802Generated: October 25, 2026

Sodium borohydride → 5-(Hydroxymethyl)thiophene-2-carbonitrile

https://huagongshe.com/reaction/725802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Formylthiophene-2-CarbonitrileHCID 12280004—
SolventEthanolHCID 702—
Product5-(Hydroxymethyl)thiophene-2-carbonitrileHCID 1060681388%

Reaction Steps

To a solution of 2-cyano-5-formyl-thiophene (6.9 g, 50 mmol) in EtOH (100 mL) was added sodium borohydride (1.9 g, 50 mmol) in portions. After 5 min of stirring, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and brine. The layers were separated and the organic phase was washed once with 1M citric acid and once with brine, then dried (MgSO4), filtered and concentrated in vacuo to give 6.1 g (88%) of 2-cyano-5-(hydroxymethyl)thiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05707966
Source datasetuspto-grants-1998_01
ORD IDord-b39e2726de21401db17e5cadc1bb0672
Source noteuspto-grants-1998_01