HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177752Generated: October 30, 2026
alpha-Bromo-2-nitrotoluene → HCID 54074348, compound
https://huagongshe.com/reaction/1177752
Participants
| Role | Name | HCID | Charge |
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| Reactant | alpha-Bromo-2-nitrotoluene | HCID 77569 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylate | HCID 2758812 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54074348 | HCID 54074348 | 13% |
Reaction Steps
To a solution of piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (8.23 g, 0.032 mol) in tetrahydrofuran (85 mL) was slowly added a solution of sodium bis(trimethylsilyl)amide (44 mL, 0.044 mol). After the resulting mixture had been stirred at −78° C. for 1 h, a solution of 2-nitrobenzyl bromide (8.21 g, 0.038 mol) was added. The reaction mixture was allowed to warm up to room temperature and was stirred overnight. It was then concentrated and the residue was partitioned between water and ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The final product was purified from the complex reaction mixture by way of column chromatography on silica gel (eluent—hexanes—ethyl acetate 4:1) to give the desired product (1.61 g, 13%) as brown oil. Mass spec.: 415.38 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842808B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-cc822867f52d4d499529a6dcee133beb |
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| Source note | uspto-grants-2010_11 |
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