HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705760Generated: October 31, 2026
Water → benzyl N-(4-bromo-2-ethylphenyl)carbamate
https://huagongshe.com/reaction/705760
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4-Bromo-2-ethylaniline | HCID 2801283 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | benzyl N-(4-bromo-2-ethylphenyl)carbamate | HCID 71232504 | — |
Reaction Steps
4-Bromo-2-ethylaniline (500 mg, 2.50 mmol) was dissolved in toluene (25 mL), sodium carbonate (397 mg, 3.75 mmol) and benzyl chloroformate (0.428 mL, 3.00 mmol) were added and the mixture stirred under nitrogen at room temperature. After 20 hours water (25 mL) was added, the aqueous phase separated and washed with ethyl acetate (2×25 mL). The combined organic extracts were washed with brine, dried over sodium sulfate and evaporated. Chromatography (40 g silica cartridge, 0-100% ethyl acetate/petroleum benzine 40-60° C.) gave the title compound (I38) (708 mg, 85%) as a pink solid; 1H NMR (400 MHz, CDCl3) δ 7.72 (s, 1H), 7.44-7.28 (m, 7H), 6.43 (s, 1H), 5.20 (s, 2H), 2.54 (q, J=7.6 Hz, 2H), 1.21 (t, J=7.6 Hz, 3H). LCMS Method C: rt 6.46 min; 258.0 [M-PhCH2O+CH3OH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174946B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-0c9c60f44436475aae1c25f7a8d8975c |
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| Source note | uspto-grants-2015_11 |
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