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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235646Generated: October 30, 2026

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

https://huagongshe.com/reaction/2235646

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 numberUS07714008B2
Source datasetuspto-grants-2010_05
ORD IDord-0948a0482211428d8ea87b76b8db2188
Source noteuspto-grants-2010_05