HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422797Generated: October 25, 2026
Diisopropylethylamine → 4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanone
https://huagongshe.com/reaction/2422797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triisopropylsilyl trifluoromethanesulfonate | HCID 2724529 | — |
| Reactant | 4-(2-Hydroxyethyl)cyclohexan-1-one | HCID 15700392 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanone | HCID 21986099 | — |
Reaction Steps
A solution of 4-(2-hydroxy-ethyl)-cyclohexanone (Intermediate R10, 6.8 g, 52.6 mmol, (obtainable as described in the publication by Ciufolini et. al. J. Amer. Chem. Soc. 1991, 113, 8016) was dissolved in CH2Cl2 (75 mL) and treated with diisopropylethylamine (9.2 mL, 52.6 mmol) followed by tri-isopropylsilyl trifluoromethane sulfonate (TIPSTf) (15.3 g, 50.2 mmol) at −30 EC. The reaction mixture was warmed to 0 EC for 1 h. The mixture was subjected to an aqueous work-up and purified by chromatography on SiO2 to give 4-(2-triisopropylsilanyloxy-ethyl)-cyclohexanone (Intermediate R11, 11.8 g (82%). Intermediate R11 was converted via Intermediate R12 to the unsaturated aldehyde, 5-(2-triisopropylsilanyloxy-ethyl)-cyclohex-1-enecarbaldehyde (Intermediate R13)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960423B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-afe455de6a624d53ad69cf55ba35721d |
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| Source note | uspto-grants-2011_06 |
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