Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyltrimethylsilane | HCID 69808 | — |
| Reactant | HCID 53709616 | HCID 53709616 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 53856743 | HCID 53856743 | 84.6% |
Reaction Steps
6-Methoxy-piperidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester (Compound 233, 1.04 g, 3.39 mmol) was dissolved in CH2Cl2 (10 mL), and the solution was cooled to −78° C. using dry ice-acetone bath. 1M TiCl4 solution in CH2Cl2 (3.7 mL) was added dropwise over a 1-minute period, followed by allyltrimethylsilane (1.61 mL, 10.14 mmol). The bath was changed to water, and the reaction mixture was stirred for 2 hours. The reaction mixture was poured into brine (50 ml) and extracted with CHCl3 (2×50 mL). The combined organic layers were washed with saturated NaHCO3 solution (50 mL) and finally dried over Na2SO4. The solvent was evaporated and the residue was purified by flash chromatography (1:5 EtOAc/hexanes) to give Compound 234 (0.91 g, 84%). Rf=0.78 (1:2 EtOAc/hexanes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630472B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-667ac87cbfa44ce4a9fd2f332101f691 |
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| Source note | uspto-grants-2003_10 |
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