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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470963Generated: October 25, 2026

Sodium borohydride → (5-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)methanol

https://huagongshe.com/reaction/470963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophene-2-carbaldehydeHCID 11277251—
SolventEthanolHCID 702—
Product(5-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)methanolHCID 57989124—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (1.74 g) was added to a solution of 5-(2-(tert-butyldimethylsilyloxy)ethyl)thiophene-2-carbaldehyde (12.4 g) (example 4, step b) in ethanol (120 mL) at 0° C. The resulting solution was stirred at 0° C. for 1 h. The reaction mixture was partitioned between brine and ethyl acetate. The organic layer was separated, dried over sodium sulphate, filtered and the solvent evaporated in vacuo to give the subtitled compound. Yield 12.1 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629271B2
Source datasetuspto-grants-2014_01
ORD IDord-4636ec5a837b4c9789240dc07af8e414
Source noteuspto-grants-2014_01