HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051863Generated: November 1, 2026
2-Chloroethyl chloroformate → HCID 68002661, compound
https://huagongshe.com/reaction/1051863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethyl chloroformate | HCID 12305 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromo-3-methoxyaniline | HCID 7018254 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68002661 | HCID 68002661 | 17.1% |
Reaction Steps
To a stirred solution of 4-Bromo-3-methoxy-aniline (10.0 g) in acetonitrile (176 mL) was added Hünig Base (25 mL) and 2-chloroethyl chloroformate (10.6 g). The mixture was stirred at room temperature for 0.5 h. The solvent was removed in vacuum. The residue was dissolved in tetrahydrofurane (250 mL), and potassium tert-butoxide (16.2 g) was added. The mixture was stirred at room temperature for 2 h. The solvent was removed in vacuum. The residue was dissolved in ethyl acetate and the mixture was washed with water and with saturated sodium chloride solution, dried (sodium sulfate) and the solvent was removed in vacuum. Silica gel chromatography gave a compound that was crystallized from ethanol. Yield: 7.7 g of the title compound. The mother liquor was concentrated in vacuum and aminophase-silica-gel chromatography gave a solid that was recrystallized from ethanol to give further 2.3 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388177B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-21cd23f96f004b469e229def0205af21 |
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| Source note | uspto-grants-2016_07 |
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