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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446392Generated: October 26, 2026

Sodium borohydride → (4-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)methanol

https://huagongshe.com/reaction/446392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2-(Tert-butyldimethylsilyloxy)ethyl)thiophene-2-carbaldehydeHCID 57989110—
SolventEthanolHCID 702—
Product(4-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)methanolHCID 58168578—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (1.40 g) was added portionwise to a stirred solution at 0° C. of 4-(2-(tert-butyldimethylsilyloxy)ethyl)thiophene-2-carbaldehyde [Aromatic Intermediate 6] (10 g) in ethanol (70 mL). The reaction mixture was stirred for 1 hour at 0° C. and then partitioned between ethyl acetate and aqueous brine and separated. The organic layer was dried, filtered and the solvent was evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 12% ethyl acetate in isohexane as solvent. Fractions containing the product were evaporated to dryness to afford the subtitled compound. Yield 6.00 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476265B2
Source datasetuspto-grants-2013_07
ORD IDord-6b9051f2312946c79a0db3d9461b4f8d
Source noteuspto-grants-2013_07