HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464580Generated: October 29, 2026
Formamidine acetate → HCID 13271775, compound
https://huagongshe.com/reaction/464580
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Butyl 8-chloro-1-phenyl-3H-2-benzazepine-5-carboxylate | HCID 13271771 | — |
| Reactant | Butyl 8-chloro-1-phenyl-5H-2-benzazepine-5-carboxylate | HCID 13271773 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13271775 | HCID 13271775 | — |
Reaction Steps
Dropwise 9.5 mL (41 mmol) of a 4.3M methanol solution of sodium methoxide was added to a solution of 8.0 g (22.6 mmol) of a mixture of 8-chloro-1-phenyl-5H-2-benzazepine-5-carboxylic acid butyl ester and 8-chloro-1-phenyl-3H-2-benzazepine-5-carboxylic acid butyl ester and 6.5 g (62.4 mmol) of formamidine acetate in 70 mL of ethanol. When the addition was complete stirring at room temperature was continued for 30 min. The reaction was diluted with water and extracted with methylene chloride. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and concentrated at reduced pressure. The residue was crystallized from a mixture of ether and petroleum ether to give a yellow solid. Recrystallization from a mixture of ether and methylene chloride gave pale yellow prisms, mp 150°-155°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04548750 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-140f7313b6ef42dc95034580338763a9 |
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| Source note | uspto-grants-1985_10 |
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