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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(2-(Tert-butyldimethylsilyloxy)ethyl)thiophene-2-carbaldehyde | HCID 57989110 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4-(2-(tert-Butyldimethylsilyloxy)ethyl)thiophen-2-yl)methanol | HCID 58168578 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476265B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-6b9051f2312946c79a0db3d9461b4f8d |
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| Source note | uspto-grants-2013_07 |
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