HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-bromo-2,3-dihydro-1H-indene-1-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(5-Bromoindane-1-ylidene)-1,3-dithiane | HCID 57419485 | — |
| Product | 5-bromo-2,3-dihydro-1H-indene-1-carboxylic acid | HCID 13840006 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592426B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-6fcbc5a141334acbbea004827b88713b |
| Source note | uspto-grants-2013_11 |