HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349775Generated: October 30, 2026
Hydrochloric Acid → HCID 11544681, compound
https://huagongshe.com/reaction/349775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Dimethylamino)phenyl isocyanate | HCID 2733372 | — |
| Reactant | (1S)-1,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione | HCID 58586461 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11544681 | HCID 11544681 | — |
Reaction Steps
To an ice-cooled solution of (1S)-1,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione (0.36 g, 2.0 mmole), triethylamine (0.20 g, 2.0 mmole) and 4-(dimethylamino)pyridine (0.24 g, 2.0 mmole) in dry dichloromethane (25 mL) was added a solution of 4-(dimethylamino)phenyl isocyanate (0.32 g, 2.0 mmole) in dry dichloromethane (5 mL). The resulting reaction mixture was allowed to stir overnight under a nitrogen atmosphere, during which time it came up to room temperature. It was then stirred at 30° C. for seven hours. The resulting mixture was treated with 2N aqueous HCl (30 mL) and the layers were separated. The acidic aqueous layer was extracted with two additional portions of dichloromethane (50 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated on a rotary evaporator. The desired product was isolated by chromatography on silica gel (10% ethyl acetate/hexane) and recrystallized from 95% ethanol to yield the title compound as a light gray solid (0.16 g, 23% yield), mp=93–95° C.; MS (−) ESI m/z=341 (M−H)−; [α]D25=−23.8° (c=1, EtOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179943B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-e332dc0945b94d8f87bd8640904e00f1 |
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| Source note | uspto-grants-2007_02 |
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