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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophene-2-carbaldehyde | HCID 11277251 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)methanol | HCID 57989124 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629271B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-4636ec5a837b4c9789240dc07af8e414 |
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| Source note | uspto-grants-2014_01 |
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