HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239228Generated: October 31, 2026
Ammonium Chloride → 1-({[tert-Butyl(diphenyl)silyl]oxy}methyl)cyclopropan-1-ol
https://huagongshe.com/reaction/2239228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]acetate | HCID 59464758 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-({[tert-Butyl(diphenyl)silyl]oxy}methyl)cyclopropan-1-ol | HCID 52987805 | 100% |
Reaction Steps
According to the description in a reference (see: Syn. Lett. 07, 1053-1054, 1999), the title compound was prepared as follows. 12 g (35 mmole) of ethyl 2-{[t-butyl(diphenyl)silyl]oxy}acetate was dissolved in 200 ml of tetrahydrofuran (THF) and 2.2 ml of titaniumtetraisopropoxide was added thereto. To the mixture was slowly added 29.2 ml of ethylmagnesiumbromide (3.0M in THF), and the reaction solution was stirred for 12 hours at room temperature. 20 ml of saturated ammonium chloride was added to stop the reaction. About 150 ml of tetrahydrofuran (THF) used as a solvent was removed by distillation under reduced pressure, and the reaction mixture was extracted twice with 200 ml of ethyl acetate. The ethyl acetate extract was distilled under reduced pressure to give 11.4 g (Yield 100%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723319B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-e0b113db60e3442391498cbcdde6319b |
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| Source note | uspto-grants-2010_05 |
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