HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042396Generated: November 1, 2026
Formamidine acetate → HCID 70926312, compound
https://huagongshe.com/reaction/1042396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | HCID 70926216 | HCID 70926216 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 70926312 | HCID 70926312 | 43% |
Reaction Steps
A 100 mL reaction flask is charged with 5,5,8,8-tetramethyl-3,4,5,6,7,8-hexahydro-2H-naphthalen-1-one (prepared as described in U.S. Pat. Nos. 3,927,083 and 2,912,462) (10 g, 0.048 mol), formamidine acetate (25 g, 0.24 mol), and butanol (50 mL). The reaction mixture is heated to 130° C. and stirred for 24 hours. The crude mass is washed once with aqueous sulfuric acid (10%, 100 mL) followed by twice with brine (30 mL). Butanol is recovered by roto-evaporation. The crude product is further purified with liquid chromatography (Biotage® system) and then crystallized. Product 7,7,10,10-tetramethyl-5,6,7,8,9,10-hexahydro-benzo[h]quinazoline (˜5 g) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557876B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-25480c98b5eb49ee84cd63ddf4f60b33 |
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| Source note | uspto-grants-2013_10 |
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