Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675307Generated: October 25, 2026

Sodium borohydride → 2-Thiophenemethanol, 5-[4-(trifluoromethyl)phenyl]-

https://huagongshe.com/reaction/1675307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(4-(Trifluoromethyl)phenyl)thiophene-2-carbaldehydeHCID 4674819—
SolventMeOH tetrahydrofuranHCID 21899815—
Product2-Thiophenemethanol, 5-[4-(trifluoromethyl)phenyl]-HCID 21986352—

Reaction Steps

To a solution of 61.2 (0.87 g, 3.40 mmol) in 3:2 MeOH/THF (25 mL) was added NaBH4 (0.13 g, 3.40 mmol) as a solid in one portion. The mixture was stirred for 2 Hours at room temperature and concentrated. The residue was suspended in 1N HCl and extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4), and concentrated to afford 61.3 as a white powder. The crude product was used without further purification. 1H NMR (400 MHz, CDCl3) δ 7.68 (d, 2H), 7.62 (d, 2H), 7.26 (d, 1H), 7.01 (d, 1H), 4.86 (d, 2H), 1.84 (t, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003648B2
Source datasetuspto-grants-2011_08
ORD IDord-fbf3afd9ea1d4c8da38cfdd0d7ad90ba
Source noteuspto-grants-2011_08