HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019841Generated: October 30, 2026
Imidazole → tert-Butyl 6-(tert-butyldimethylsilyloxy)hexylcarbamate
https://huagongshe.com/reaction/1019841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | tert-Butyl N-(6-hydroxyhexyl)carbamate | HCID 4146612 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 6-(tert-butyldimethylsilyloxy)hexylcarbamate | HCID 86676514 | 87% |
Reaction Steps
To a solution of tert-butyl 6-hydroxyhexylcarbamate (21 mmol) in CH2Cl2 (30 ml) was added imidazole (27 mmol) at 0° C. The reaction mixture was kept at 25° C. and stirred for 20 min, then cooled to 0° C. To the resulting reaction mixture was added tert-butyldimethylchlorosilane (23 mmol) dropwise over 30 min at 0° C. The reaction mixture was allowed to warm to 25° C. and stirred for 16 h and then filtered. The filtrate was washed with 1 N HCl (2×25 ml) and brine (30 ml), dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was purified by SiO2 flash column (eluent: petroleum ether and then CH2Cl2). Yield 6.53 g (87% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716293B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-b9f519400d5e4537b17781dabf7aa039 |
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| Source note | uspto-grants-2014_05 |
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