Phosphoric Acid → 1-Methyl-3-phenyl-2,3-dihydro-1H-indene

HRID 1973850Notes

Reaction equation

HRID 1973850 reaction equation
Cl[C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[CH2:5].Cl[CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.P(=O)(O)(O)O.C=CC1C=CC=CC=1>>[CH3:11][CH:12]1[C:13]2[C:18](=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:4]([C:3]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:2]=2)[CH2:5]1

Participants

5

Procedure

A mixture of 115 parts of o-chlorostyrene and 35 parts of o-chloroethylbenzene is added to 652 parts of 89 per cent strength by weight aqueous phosphoric acid at 40° to 45° C whilst stirring vigorously. A mixture of 90 parts of styrene, 115 parts of o-chlorostyrene and 35 parts of o-chloroethylbenzene is added to the resulting emulsion at a temperature of 40° to 45° C over 5 hours. After completion of the addition, the mixture is stirred for a further 2 hours at 40° to 45° C. The organic phase is separated off, washed with 200 parts of 3 per cent strength by weight sodium hydroxide solution and fractionated. 24.9 parts of 1-methyl-3-phenylindan (b.p. 145° to 146° C (10 mm)), 63.1 parts of 1-methyl-3-(o-chloro)-phenylindan (b.p. 165° to 168° C (10 mm), nD25 : 1.5890) and 31 parts of 1-methyl-3-(o-chloro)-phenyl-7-chloroindan (b.p. 195° to 200° C (10 mm)) are isolated.

Workup

  1. additionis added to the resulting emulsion at a temperature of 40° to 45° C over 5 hours
  2. additionAfter completion of the addition
  3. stirringthe mixture is stirred for a further 2 hours at 40° to 45° C
  4. customThe organic phase is separated off
  5. washwashed with 200 parts of 3 per cent strength by weight sodium hydroxide solution

Sources & evidence

ORD record
ord-c2bd80c93eec49529970ce69c1f9c3c6
Source dataset
uspto-grants-1976_12
Patent number
US03998894

Reaction notes

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