HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443273Generated: October 30, 2026
m-Xylyl bromide → HCID 21193326, compound
https://huagongshe.com/reaction/443273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Xylyl bromide | HCID 12099 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 4-Benzyl 1-tert-butyl piperidine-1,4-dicarboxylate | HCID 22255913 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21193326 | HCID 21193326 | — |
Reaction Steps
To a cold (-78° C.) solution of benzyl N-tert-butoxycarbonyl-isonipecotate (8.02 g, 25.11 mmol) in anhydrous THF (80 mL), a solution of sodium bis(trimethysilyl)amide (35 mL, 35 mmol; 1M) in THF was added over a period of 10 min. The resulting orange solution was stirred at -78° C. for 1 h. and then treated dropwise with 3-methylbenzyl bromide (4.1 mL, 30.6 mmol). The reaction mixture was allowed to warm to room temp., and stirred overnight. The reaction was quenched with saturated aqueous ammonium chloride, diluted with water, and extracted with ethyl acetate. The organic extracts were combined, washed with brine, and concentrated under vacuum. The residual oil was subjected to column chromatography on silica eluting with 20% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891889 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-f64c3a42dfd44820bd1b4599428ee5a2 |
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| Source note | uspto-grants-1999_04 |
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