HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367311Generated: October 30, 2026
Ammonium Chloride → HCID 178430664, compound
https://huagongshe.com/reaction/367311
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 178475393 | HCID 178475393 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178430664 | HCID 178430664 | 37% |
Reaction Steps
Under a nitrogen atmosphere, 0.98 g of 1-amino-3-[(5-acetoxy-4,6-di-t-butyl-2-methyl-2,3-dihydrobenzofuran-2-yl)methyl]guanidine was dissolved in 50 ml of toluene. To the solution was added 10 ml of diisobutyl aluminum hydride (1.0 M in toluene) and the mixture was stirred at room temperature for 1 hour. After reaction, a saturated aqueous ammonium chloride solution was added and insoluble matters were filtered off on Celite. The filtrate was 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 0.32 g of 1-amino-3-[(4,6-di-t-butyl-5-hydroxy-2-methyl-2,3-dihydrobenzofuran-2-yl)methyl]guanidine as a white crystal (yield 37%).
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-292d3a22c74e4b62b891b756023efcca |
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| Source note | uspto-grants-2000_10 |
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