HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435450Generated: October 30, 2026
Ammonium Chloride → HCID 70533072, compound
https://huagongshe.com/reaction/435450
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 12918300 | HCID 12918300 | — |
| Reactant | HCID 70533310 | HCID 70533310 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70533072 | HCID 70533072 | 109.3% |
Reaction Steps
To a stirred solution of 1-trimethylsilyl-N-benzylidene-3-aminoprop-1-yne (7.609 g.; 34.4 mmol) in 106 ml. of tetrahydrofuran maintained at -78° under N2 was added dropwise 19.5 ml. of 1.63 N n-butyl lithium. To the stirred deep red solution was then added dropwise 11.43 g. (35.4 mmol) of 3,4-diphenylmethylenedioxybenzyl chloride in 35 ml. of tetrahydrofuran. After an additional 30 minutes at -78° water (25 ml.) was added dropwise, the mixture was warmed to 20°, 10% aqueous NH4Cl solution was added and the layers were separated. The aqueous layer was washed twice with benzene, the combined organic phases were washed twice with cold 10% aqueous NH4Cl, once with saturated NaCl solution, dried over Na2SO4 and concentrated to dryness to give 3-(3,4-diphenylmethylenedioxybenzyl)-1-trimethylsilyl-N-benzylidene-3-aminoprop-1-yne as a viscous orange oil (18,86 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04401676 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-84b54e3d7ee84c409d5e70fbfe640e14 |
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| Source note | uspto-grants-1983_08 |
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