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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453024Generated: October 31, 2026

Methyl Isocyanate → HCID 58762667, compound

https://huagongshe.com/reaction/1453024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
Reactant(R)-4-bromo-alpha-methylbenzylamineHCID 853000—
SolventDichloromethaneHCID 6344—
ProductHCID 58762667HCID 5876266794%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of (R)-(+)-1-(4-bromophenyl)ethylamine (0.5 g, 2.49 mmol) in anhydrous CH2Cl2 was added methyl isocyanate (0.15 mL, 2.49 mmol). The resulting solution was stirred at 25° C. overnight. CH2Cl2 was evaporate and residue partitioned between EtOAC and 1N HCl. The organic layer was washed with H2O, brine and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by flash column chromatography (80% EtOAc in hexanes) to provide the desired product (0.60 g, 94%) as a white solid. 1H NMR (CDCl3) δ: 1.42 (d, J=7.0 Hz, 3H), 2.72 (d, J=4.9 Hz, 3H), 4.25 (brs, 1H), 4.73 (brs, 1H), 4.74-4.81 (m, 1H), 7.20 (d, J=8.3 Hz, 2H), 7.45 (d, J=8.3 Hz, 2H). ESIMS (MNa+): 258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-d2a9f0ae6f48415e920c4c6ae46cc4f6
Source noteuspto-grants-2009_01