HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → [4-Bromo-2-(2-bromoacetyl)phenoxy]acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 2-(2-acetyl-4-bromophenoxy)acetate | HCID 19261366 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | [4-Bromo-2-(2-bromoacetyl)phenoxy]acetic acid ethyl ester | HCID 57658801 | 94% |
Reaction Steps
To a cooled (0° C.) solution of (2-acetyl-4-bromophenoxy)acetic acid ethyl ester (2.5 g, 8.3 mmol) in CHCl3 (25 mL) was slowly added bromine (425 uL, 8.3 mmol). After completion the reaction mixture was allowed to stir at room temperature for 1 hour. The mixture was partitioned between CH2Cl2 and brine. The organic phase was washed with brine, dried (MgSO4) and concentrated in vacuo to give the title compound as a white solid (2.97 g, 7.8 mmol, 94%): 1H NMR (CDCl3): δ 1.35 (t, 3H), 4.32 (q, 2H), 4.75 (s, 2H), 4.76 (s, 2H), 6.77 (d, 1H), 7.60 (dd, 1H), 7.97 (s, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022063B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-362a6e885afd4e0ab0c31f51c8644df9 |
| Source note | uspto-grants-2011_09 |