HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70245Generated: October 27, 2026
Dimethylformamide → Methyl [(2-chloro-5-iodo-phenyl)methyl]carbamate
https://huagongshe.com/reaction/70245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Bromomethyl)-1-chloro-4-iodobenzene | HCID 11739038 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl [(2-chloro-5-iodo-phenyl)methyl]carbamate | HCID 66789912 | — |
Reaction Steps
To a mixture of potassium carbonate (4.30 g, 53.3 mmol) in N,N-dimethylformamide (47 mL) and methanol (5 mL) at 50° C. was added a solution of 2-(bromomethyl)-1-chloro-4-iodobenzene (i.e. the product of Step A) (5.20 g, 15.7 mmol) in N,N-dimethylformamide (10 mL). The reaction mixture was heated at 110° C. for 1 h and then cooled to room temperature. The reaction mixture was partitioned between diethyl ether (200 mL) and water (200 mL), the organic layer was separated, washed with water (3×50 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to provide the title compound as a yellow oil (4.32 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822521B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-b3fe1e5ffa074e2094d4611176128ea7 |
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| Source note | uspto-grants-2014_09 |
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