HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215942Generated: October 27, 2026
1-Bromo-2-Chloroethane → 1-Benzyl 4-methyl 4-(2-chloroethyl)piperidine-1,4-dicarboxylate
https://huagongshe.com/reaction/215942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | 1-Benzyl 4-methyl piperidine-1,4-dicarboxylate | HCID 1512544 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzyl 4-methyl 4-(2-chloroethyl)piperidine-1,4-dicarboxylate | HCID 58893184 | — |
Reaction Steps
Lithium bis(trimethylsilyl)amide (LiHMDS) in THF (1.0 M, 7.2 mL, 0.0072 mol) was added to a solution of 1-benzyl 4-methyl piperidine-1,4-dicarboxylate (1.00 g, 0.00360 mol) in tetrahydrofuran (10.0 mL) at −78° C. The reaction mixture had been stirred at −78° C. for 1 hr, then 1-bromo-2-chloroethane (0.45 mL, 0.0054 mol) was slowly added to the mixture. The reaction mixture was allowed to warm to room temperature and stirred for 2 hrs. The reaction was quenched with saturated NH4Cl, extracted with ethyl acetate. The combined organic layers were dried over Na2SO4, filtered, concentrated. The residue was flash chromatographed (ethyl acetate in hexane: 20%) to afford 1-benzyl 4-methyl 4-(2-chloroethyl)piperidine-1,4-dicarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193207B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-a415cabdb7e14f55bef4e499903a0012 |
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| Source note | uspto-grants-2012_06 |
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