HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531463Generated: October 25, 2026
Sodium hydride → Tert-butyl 4-(3-bromobenzylidene)piperidine-1-carboxylate
https://huagongshe.com/reaction/531463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 3-Bromobenzyl bromide | HCID 69979 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Tert-butyl 4-(3-bromobenzylidene)piperidine-1-carboxylate | HCID 57813409 | 51.5% |
Reaction Steps
The mixture of 1-bromo-3-(bromomethyl)benzene (6.2 g, 24.8 mmol) and triethyl phosphite (4.53 g, 27.28 mmol) was heated at 90° C. for 12 hours, cooled to 0° C., added DME (40 ml) and tert-butyl 4-oxopiperidine-1-carboxylate (5.73 g, 28.8 mmol) and sodium hydride (1.19 g, 49.6 mmol) and stirred at RT for 2-3 hours. Diluted with water and extracted with ether to afford 4.5 g (51.5% yield) of the titled product after purification with (60/120 silica gel) column chromatography using 10% ethyl acetate in hexane as eluent. MS: m/z=353.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353107B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-7449a3134678448683907a8a825d8072 |
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| Source note | uspto-grants-2016_05 |
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