HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520414Generated: October 25, 2026
Diisopropylamine → Tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilane
https://huagongshe.com/reaction/520414
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Propanoic acid, 2-methoxy-, methyl ester | HCID 86599 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilane | HCID 86130319 | — |
Reaction Steps
A solution of methyl 2-methoxypropionate (177 mg, 1.5 mmol) in THF (1 mL) was added to a solution of LDA prepared from diisopropylamine (0.212 mL, 1.50 mmol) and butyllithium (0.60 mL, 1.50 mmol) in THF (2 mL) at −78° C. under nitrogen. The mixture was gradually allowed to warm to −20° C. over 1 h, re-cooled to −78° C. and then a solution of tert-butylchlorodimethylsilane (233 mg, 1.50 mmol) in THF (1 mL) was added. The mixture was allowed to warm to rt over 2 h and stirred overnight. The reaction was quenched with satd. NaHCO3 (5 mL), diluted with DCM (10 mL). The organic layer was separated, washed with water, brine and dried (MgSO4). Evaporation of solvents afforded tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilane as a clear oil and used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326973B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-842df4223b95441b84cabe8d66a92937 |
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| Source note | uspto-grants-2016_05 |
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