HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463320Generated: November 1, 2026
Sodium hydride → 5-(t-Butyldimethylsilyloxy)pent-1-yne
https://huagongshe.com/reaction/1463320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 4-Pentyn-1-ol | HCID 79346 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-(t-Butyldimethylsilyloxy)pent-1-yne | HCID 10867306 | 96% |
Reaction Steps
To a suspension of 18.0 g (749 mmol, 1.05 equiv.) of sodium hydride in 500 mL of THF at 0° C. was added a solution of 60.0 g (713 mmol, 1.00 equiv.) of 4-pentyne-1-ol in 150 mL of THF. When the addition was complete the reaction was allowed to warm to room temperature over one hour. To this mixture was added 113 g (749 mmol, 1.05 equiv.) of t-butyldimethylsilyl chloride in 150 mL of THF. The reaction was allowed to stir for 16 hours at room temperature then diluted with 1200 mL of hexane. The organic layer was washed with 500 mL of saturated aqueous sodium bicarbonate, dried over anhydrous sodium sulfate and concentrated in vacuo. The resulting liquid was distilled at 39°-42° C. at 0.05 mm Hg to yield 135 g (96%) of 1-t-butyldimethylsilyloxy-4-pentyne
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05300506 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-f213dce00f3b4fa1a357d39b44e79ef6 |
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| Source note | uspto-grants-1994_04 |
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