HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-Bromo-3-(3,4-dichloro-phenyl)-propionaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | 3-(3,4-Dichlorophenyl)propanal | HCID 23499572 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Bromo-3-(3,4-dichloro-phenyl)-propionaldehyde | HCID 58126840 | — |
Reaction Steps
To a solution of the product of example 37 (10 mmol, 2.0 g) in a mixed solvent of DCM (40 ml) with dioxane (4.0 ml) was added TMSBr (15 mmol, 2.3 g) at room temperature. After the mixture was kept at 25° C. for one hour, bromine (1.6 g, 10.0 mmol) was added. Another one hour later, the mixture was poured into water (50 ml) and extracted with DCM three times. The combined organic layers were washed with brine, dried and evaporated into dryness to give the crude title product, which was used directly in the next step reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431581B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-35dcfee7547d485687e67748015325b2 |
| Source note | uspto-grants-2013_04 |