HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(3-Bromo-2-hydroxy-5-methylphenyl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Hydroxy-5-methylacetophenone | HCID 15068 | — |
| Reactant | Bromine | HCID 24408 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Bromo-2-hydroxy-5-methylphenyl)ethan-1-one | HCID 11138918 | 48% |
Reaction Steps
To a solution of 21.5 g (0.143 mol) of 20 in 40 mL of dry dichloromethane, 0.3 g of iron turnings was added, and then a solution of 10.7 mL (34.2 g, 0.215 mol) of bromine in 100 mL of dichloromethane was added dropwise by vigorous stirring for 20 min. This mixture was refluxed for 30 min, and then 300 mL of water was added. The organic layer was separated, and the aqueous layer was extracted with 2×100 mL of dichloromethane. The combined organic extract was washed by saturated aqueous Na2SO3, dried over K2CO3, and then evaporated to dryness. Rectification of the residue in vacuum gave 15.7 g (48%) of the title product (bp 105-115° C./1 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557936B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-cb559e5603004aa794e67acf466603f6 |
| Source note | uspto-grants-2013_10 |