HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193635Generated: November 1, 2026
2-Chloroethyl isocyanate → HCID 49855325, compound
https://huagongshe.com/reaction/2193635
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroethyl isocyanate | HCID 16035 | — |
| Reactant | 2-Methoxybenzylamine | HCID 81292 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 49855325 | HCID 49855325 | 67.8% |
Reaction Steps
Commercially available 2-chloroethylisocyanate (3.10 mL, 36.45 mmol) was added slowly to a solution of 2-methoxybenzylamine (5.00 mL, 36.45 mmol) in dichloromethane (60 mL) at room temperature. The resulting reaction mixture was stirred for 30 minutes and the intermediate product thus formed was filtered and washed with hexane, and then suspended in water (150 mL). This suspension was heated to reflux and stirred at refluxing for 2 hours, then cooled to room temperature. The reaction mixture was extracted with ethyl acetate, and the aqueous phase was basified with ammonium hydroxide to pH=14. The basified aqueous phase was then extracted with ethyl ether (50 mL) 3 times and the combined organic phases were dried with magnesium sulfate. Concentration gave 5.10 g of N-(2-methoxybenzyl)-4,5-dihydrooxazol-2-amine. Spectroscopic data: 1H NMR (300 MHz, CDCl3) δ=3.80 (t, 2H, J=10.1 Hz), 3.85 (s, 3H), 4.26 (t, 2H, J=10.1 Hz), 4.38 (s, 2H), 6.83-6.95 (m, 2H), 7.20-7.32 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329918B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-9a75ca0ae23b4dbda2b9cf0b434ebc65 |
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| Source note | uspto-grants-2012_12 |
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