HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569211Generated: October 30, 2026
Benzyl Chloride → HCID 14716816, compound
https://huagongshe.com/reaction/569211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | N-tert-Butyl-3-methylpyridine-2-carboxamide | HCID 5463796 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14716816 | HCID 14716816 | 94% |
Reaction Steps
Tetrahydrofuran (125 mL), N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide (1 equivalent) and sodium bromide (1.3 g) are charged and cooled to -40° C. under nitrogen. Two equivalents of n-butyllithium are then added over 40 minutes. When half the n-butyllithium is added the mixture turns purple. Benzyl chloride (1.05 equivalents) is then added dropwise (1:1 solution in tetrahydrofuran) over 40-50 minutes while the temperature is maintained at -40° C. After 30 minutes at -40° C., the mixture is diluted with water (250 ml) and the organic phase separated. This phase is dried over sodium sulphate and the solvent removed yielding an oil from which solid product may crystallize. Product yield of 94% determined by internal standard assay on gas chromatograph.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731447 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-5865e0f1508248c39f9f2b3fae5a0b21 |
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| Source note | uspto-grants-1988_03 |
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