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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046553Generated: October 25, 2026

Acetic Acid → 5-bromo-2,3-dihydro-1H-indene-1-carboxylic acid

https://huagongshe.com/reaction/2046553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant2-(5-Bromoindane-1-ylidene)-1,3-dithianeHCID 57419485—
Product5-bromo-2,3-dihydro-1H-indene-1-carboxylic acidHCID 1384000686%

Reaction Steps

To a mixture of 2-(5-bromo-indan-1-ylidene)-[1,3]dithiane (2.02 g, 6.45 mmol) in acetic acid (34 ml) was added 37% HCl (11 ml). After the addition, the brown mixture was heated to reflux for 3 h; then, the reaction mixture was allowed to cool to room temperature and was concentrated to dryness, using toluene as co-evaporating solvent to remove acetic acid and water. This process was repeated four times. The remaining brown oil was purified by chromatography (silica gel; CH2Cl2/EtOAc 100:0-0:100) to obtain the title compound as light brown solid (1.335 g, 86%). MS: 238.6 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592426B2
Source datasetuspto-grants-2013_11
ORD IDord-6fcbc5a141334acbbea004827b88713b
Source noteuspto-grants-2013_11