HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651127Generated: November 4, 2026
Menthyl chloroformate → HCID 14850317, compound
https://huagongshe.com/reaction/1651127
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Menthyl chloroformate | HCID 151928 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 10383090 | HCID 10383090 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14850317 | HCID 14850317 | 74.4% |
Reaction Steps
To a cold (-78° C.) solution of 2-[(4-bromo-2-fluorophenyl)methyl]-1,3(2H, 3H)-isoquinolinedione (9.0 g, 25.86 mmol) in anhydrous THF (120 mL) was added lithium bis(trimethylsilyl)amide (1.0M solution in THF, 56.91 mL, 56.91 mmol), dropwise over a 10 minute period. After stirring for 3 hours, (-)menthyl chloroformate (8.48 mL, 38.79 mmol) was added and the reaction was allowed to warm up to room temperature. The mixture during that period turned a dark color. It was stirred an additional 30 minutes and quenched with H2O. The dark solution was poured into H2O, acidified with HCl (2N) and extracted with EtOAc. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography on acid-washed silica gel (5% H3PO4 in MeOH) gave a clear oil (10.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04927831 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-ab1c15b63a9b41ffa9018621958846c0 |
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| Source note | uspto-grants-1990_05 |
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