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Hydrochloric Acid → Hexane, 2,5-dichloro-2,5-dimethyl-

HRID 492284
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HRID 492284 반응식
[CH3:1][C:2](O)([CH2:4][CH2:5][C:6]([CH3:9])(O)[CH3:7])[CH3:3].[ClH:11].O.C(Cl)[Cl:14]>>[Cl:11][C:2]([CH3:3])([CH2:4][CH2:5][C:6]([Cl:14])([CH3:9])[CH3:7])[CH3:1]
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참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 6344DichloromethaneHCID 80312,5-Dimethyl-2,5-hexanediol

생성물 1

HCID 80360Hexane, 2,5-dichloro-2,5-dimethyl-수율 87%

실험 절차

To 2,5-dimethyl-2,5-hexanediol (10 g, 68.5 mmol) in a 500 mL flask was added reagent grade concentrated HCl (150 mL) and the solution was stirred at ambient temperature for 1 h. Water (100 mL) and CH2Cl2 (100 mL) were then added slowly and the layers were separated. The aqueous layer was washed with additional CH2Cl2 (100 mL). The combined organic layers were dried over MgSO4 and filtered thru silica gel pad. The solvent was removed to yield 10.9 g (87%) of 2,5-dichloro-2,5-dimethylhexane. The dichloride was dissolved in 150 mL of CH2Cl2 and 9.6 mL of toluene (90 mmol) was added. AlCl3 (390 mg, 2.9 mol) was added in portions over 5 min at ambient temperature. HCl is evolved and the solution tums dark red. The reaction was placed in an ice-bath and quenched with deionized water (120 mL). Hexane (150 mL) was added and the organic layer was removed. The aqueous layer was washed with additional hexane (150 mL). The combined organic layers were washed with water (200 mL) and brine (100 mL) and dried over MgSO4. The solvent was removed in vacuo to give 1,1,4,4,6-pentamethyl-1,2,3,4-tetrahydronaphthalene as a colorless oil that crystallized after storage at −20° C.

후처리

  1. customthe layers were separated
  2. washThe aqueous layer was washed with additional CH2Cl2 (100 mL)
  3. dry with materialThe combined organic layers were dried over MgSO4
  4. filtrationfiltered
  5. customThe solvent was removed

출처 및 근거

ORD 기록
ord-dd60547ae806453bab7b2d2912836249
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07531695B2

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