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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834668Generated: November 1, 2026

Bromine → (1-Oxo-2-bromo-2-ethyl-6,7-dichloro-5-indanyloxy)acetic acid

https://huagongshe.com/reaction/1834668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantAcetic acid, 6,7-dichloro-2-ethyl-1-oxo-5-indanyloxy-HCID 33794—
ReactantSodium BisulfiteHCID 23665763—
CatalystHydrogen BromideHCID 260—
SolventAcetic AcidHCID 176—
Product(1-Oxo-2-bromo-2-ethyl-6,7-dichloro-5-indanyloxy)acetic acidHCID 2037391597%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04070539
Source datasetuspto-grants-1978_01
ORD IDord-9157501c0de64555aa35d52bda3eca4b
Source noteuspto-grants-1978_01