1-(2,3-Dihydro-1H-inden-5-yl)ethan-1-one → 2,3-dihydro-1H-indene-5-carboxylic acid

HRID 2038112Notes

Reaction equation

HRID 2038112 reaction equation
Cl[O-].[Na+].[CH2:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13](=[O:15])C)[CH:11]=2)[CH2:6][CH2:5]1.C([O-])(O)=[O:17].[Na+]>>[CH2:6]1[C:7]2[C:12](=[CH:11][C:10]([C:13]([OH:15])=[O:17])=[CH:9][CH:8]=2)[CH2:4][CH2:5]1

Participants

4

Reactant 3

HCID 2339761-(2,3-Dihydro-1H-inden-5-yl)ethan-1-oneHCID 516892Sodium BicarbonateHCID 23665760Sodium Hypochlorite

Product 1

HCID 2328412,3-dihydro-1H-indene-5-carboxylic acidYield 99%

Conditions

Temperature
55 °C

Procedure

To a stirred aqueous sodium hypochlorite solution (2230 ml, 1.80 mmol, 6%) at 55° C. was added 1-(2,3-dihydro-1H-inden-6-yl)ethanone (120.0 g, 0.75 mol) and the mixture was stirred at 55° C. for 2 h. After cooling to room temperature, saturated NaHCO3 solution was added until the solution became clear. The produced precipitate was filtered, washed several times with water and dried to afford the desired product (120.0 g, 99%). 1 H NMR (CDCl3, 300 MHz) δ 2.07-2.17(m, 2H), 2.96(t, J=7.5 Hz, 4H), 7.30(d, J=7.8, 111,), 7.91(d, J=7.8, 1H), 7.96(s, 1H).

Workup

  1. temperatureAfter cooling to room temperature
  2. filtrationThe produced precipitate was filtered
  3. washwashed several times with water
  4. customdried

Sources & evidence

ORD record
ord-82bb20d499424dd4a61a66cf0c7c92f1
Source dataset
uspto-grants-2013_11
Patent number
US08575209B2

Reaction notes

Loading…