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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972753Generated: November 3, 2026

1,3-Dibromo-5,5-dimethylhydantoin → HCID 58529693, compound

https://huagongshe.com/reaction/1972753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantHCID 58529955HCID 58529955—
SolventDimethylformamideHCID 6228—
ProductHCID 58529693HCID 58529693194.6%

Reaction Conditions

Temperature-20 °C

Reaction Steps

The product of step 6 (3.59 g, 10.22 mmoL) was dissolved in 40 mL of DMF and cooled in an Ice/isopropanol/dry ice bath to −20° C. and 1,3-dibromo-5,5-dimethylhydantoin (1.46 g, 5.11 mmol) was added in 4 equal portions 15 minutes apart. The mixture was stirred for 10 minutes past the last addition and quenched by addition to a mixture of ice (400 g), saturated, aqueous Na2SO3 (20 mL) and 2M aq. Na2CO3 (20 mL) and the mixture was allowed to reach rt and vigorously stirred for 30 minutes. The solid was collected by filtration dried in a vacuum oven until a constant weight was obtained. The title compound (4.28 g) was obtained as a freely flowing solid. 1H NMR (300 MHz, CD3OD) δ 7.83 (s, 1H), 7.40-7.25 (m, 5H), 6.66 (s, 1H), 5.06 (bs, 2H), 4.19 (d, 1H), 3.92 (m, 1H), 3.22 (m, 1H), 3.12-2.83 (m, 3H), 1.99, (m, 1H), 1.78-1.62 (m, 2H), 1.48 (m, 1H). ES-MS m/z 430.1, 432.0 [M+H]+, HPLC RT (min) 2.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-5e7b25d116e9492c93759dbfa23dc2c3
Source noteuspto-grants-2013_04