HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399324Generated: October 30, 2026
1,5-Pentanediol → HCID 18970864, compound
https://huagongshe.com/reaction/399324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Pentanediol | HCID 8105 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18970864 | HCID 18970864 | — |
Reaction Steps
A solution of 1,5-pentandiol (44 mmol) in THF (15 mL) is cooled to 0° C. and treated with sodium hydride (44 mmol) followed by tert-butyldimethylsilyl chloride (44 mmol). The reaction mixture is stirred at room temperature overnight. Concentration in vacuo and flash chromatography affords 5-trimethylsiloxy-1-pentanol. To a solution of 5-trimethylsiloxy-1-pentanol (11.6 mmol) in dry dichloromethane (50 mL) is added 2,6-di-tert-butyl-4methylpyridine (4.6 g, 22.2 mmol) and triflic anhydride (3.7 mL, 22.2 mmol) at 0° C. The reaction is stirred at room temperature for 20 min, poured into water, and extracted with dichloromethane. The combined extracts are dried over anhydrous sodium sulfate and concentrated in vacuo and to afford 5-trimethylsiloxy-1-pentyl triflate (45) which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05817879 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-74b7192603964530afc066f65a969a50 |
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| Source note | uspto-grants-1998_10 |
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