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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895809Generated: October 30, 2026

Sodium borohydride → HCID 57319589, compound

https://huagongshe.com/reaction/1895809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12539266HCID 12539266—
SolventMethanolHCID 887—
ProductHCID 57319589HCID 5731958989.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-vinyl-thiophene-2-carbaldehyde (900 mg, 6.4 mmol) in anhydrous methanol (20 mL) was cooled to 0° C. under an atmosphere of nitrogen and treated with sodium borohydride (268 mg, 7.1 mmol). The reaction was stirred at 0° C. for 5 minutes and then at room temperature for 5 minutes, before being quenched with water and concentrated in vacuo. The aqueous layer was extracted twice with dichloromethane, the combined organics dried through a hydrophobic frit and concentrated in vacuo. The product was purified by silica gel chromatography using iso-hexanes/ethyl acetate 7:1 then 2:1 to afford the title compound (800 mg, 88%) as a colourless oil. 1H NMR (300 MHz, CDCl3) δ1.76 (t, J=6.0 Hz, 1H), 4.80 (d, J=6.3 Hz, 2H), 5.15 (d, J=10.7 Hz, 1H), 5.55 (d, J=17.4 Hz, 1H), 6.78 (dd, J=17.4, 10.7 Hz, 1H), 6.85 (d, J=3.6 Hz, 1H), 6.88 (d, J=3.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513184B2
Source datasetuspto-grants-2013_08
ORD IDord-018744c726ef49e8bda651ac22444d9c
Source noteuspto-grants-2013_08