HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → (1-Oxo-2-bromo-2-ethyl-6,7-dichloro-5-indanyloxy)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Acetic acid, 6,7-dichloro-2-ethyl-1-oxo-5-indanyloxy- | HCID 33794 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Hydrogen Bromide | HCID 260 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (1-Oxo-2-bromo-2-ethyl-6,7-dichloro-5-indanyloxy)acetic acid | HCID 20373915 | 97% |
Reaction Steps
To a stirred suspension of (1-oxo-2-ethyl-6,7-dichloro-5-indanyloxy)acetic acid (30.3 g., 0.10 moles) in acetic acid (300 ml.) is added a solution of bromine (16.0 g., 0.10 moles) in acetic acid (50 ml.) over a period of 30 minutes. The reaction is catalyzed by the addition of 48% aqueous hydrobromic acid (2 drops). The clear yellow solution is stirred at room temperature for 30 minutes then poured into ice water (1 l.) containing sodium bisulfite (2 g.). The crude (1-oxo-2-bromo-2-ethyl-6,7-dichloro-5-indanyloxy)acetic acid (36 g., 97%) thus obtained is filtered, washed with water and dried. It melts at 189°-191° C. after recrystallization from a mixture of ethyl acetate and hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04070539 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-9157501c0de64555aa35d52bda3eca4b |
| Source note | uspto-grants-1978_01 |