HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367319Generated: October 30, 2026
Ammonium Chloride → HCID 178431197, compound
https://huagongshe.com/reaction/367319
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178475395 | HCID 178475395 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178431197 | HCID 178431197 | 25.1% |
Reaction Steps
Under a nitrogen atmosphere, 2.0 g of 1-{4-[(5-acetoxy-4,6-di-t-butyl-2-methyl-2,3-dihydrobenzofuran-2-yl)methoxy]benzylideneamino}guanidine was dissolved in 100 ml of tetrahydrofuran, and 10 ml of n-butyl lithium (1.6 M in n-hexane) was added and the mixture was stirred at room temperature for 30 minutes. After reaction, the reaction solution was combined with a saturated aqueous ammonium chloride solution and extracted with ethyl acetate, and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated. The concentrate was purified by silica gel column chromatography eluting with chloroform containing 10% methanol to give 0.46 g of 1-{4-[(4,6-di-t-butyl-5-hydroxy-2-methyl-2,3-dihydrobenzofuran-2-yl)methoxy]benzylideneamino}guanidine as a pale yellow solid (yield 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133279 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-502e1f88ca0a4ec5a6c4c26b2e52a258 |
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| Source note | uspto-grants-2000_10 |
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