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2-Cyclopentyl-1-(2,3-dichloro-4-methoxyphenyl)prop-2-en-1-one → 6,7-dichloro-2-cyclopentyl-5-methoxy-2,3-dihydro-1H-inden-1-one

HRID 358270
Notes
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Reaction equation

HRID 358270 reaction equation
[CH:1]1([C:6](=[CH2:19])[C:7]([C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([Cl:17])[C:10]=2[Cl:18])=[O:8])[CH2:5][CH2:4][CH2:3][CH2:2]1>S(=O)(=O)(O)O>[Cl:17][C:11]1[C:10]([Cl:18])=[C:9]2[C:14]([CH2:19][CH:6]([CH:1]3[CH2:5][CH2:4][CH2:3][CH2:2]3)[C:7]2=[O:8])=[CH:13][C:12]=1[O:15][CH3:16]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 123955522-Cyclopentyl-1-(2,3-dichloro-4-methoxyphenyl)prop-2-en-1-one

Product 1

HCID 123955576,7-dichloro-2-cyclopentyl-5-methoxy-2,3-dihydro-1H-inden-1-one

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Conditions

Temperature
20 °C

Procedure

4-(2-Cyclopentyl-2-methyleneacetyl)-2,3-dichloroanisole (33.3 g.) is dissolved in 98% sulfuric acid (150 ml.) and stirred at 20° C. for 1.5 hours. The solution then is added dropwise with stirring to ice water. The aqueous phase is decanted from the gummy product and fresh water is added. After 20 hours the gum solidifies and is crystallized from hexane-benzene (3:1) to obtain 6,7-dichloro-2-cyclopentyl-2,3-dihydro-5-methoxy-1H-inden-1-one, m.p. 116°-117° C.

Workup

  1. additionThe solution then is added dropwise
  2. customThe aqueous phase is decanted from the gummy product and fresh water
  3. additionis added
  4. waitAfter 20 hours the gum solidifies
  5. customis crystallized from hexane-benzene (3:1)

Sources & evidence

ORD record
ord-fb796cc370e247b490e555e2511e6ebc
Source dataset
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04465850

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes