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
Participants
| Role | Name | HCID | Charge |
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| 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 | 97.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133185B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-37e18061e48e4fd6916b5894870ddf5a |
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| Source note | uspto-grants-2015_09 |
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