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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279957Generated: November 2, 2026

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

https://huagongshe.com/reaction/2279957

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 5798912497.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-[2-[tert-butyl(dimethyl)silyl]oxyethyl]thiophene-2-carbaldehyde (17.8 g, 66.1 mmol) in ethanol (180 mL) at 0° C. was added sodium borohydride (2.5 g, 66.1 mmol). The resulting solution was stirred at 0° C. for 1.5 h. The reaction solution was concentrated in vacuo and partitioned between ethyl acetate (30 mL) and brine (30 mL). The organic phase was over sodium sulphate, filtered and concentrated in vacuo to give the title compound as a yellow oil (17.5 g, 97%) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133185B2
Source datasetuspto-grants-2015_09
ORD IDord-37e18061e48e4fd6916b5894870ddf5a
Source noteuspto-grants-2015_09