Chlorobutanol → 4-Chloro-1-(naphthyloxy)-2-butanol

HRID 64692

Reaction equation

HRID 64692 reaction equation
[C:1]1([OH:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[OH-].[K+].Cl[CH2:15][CH:16]([OH:20])[CH2:17][CH2:18][Cl:19].CC(O)(C(Cl)(Cl)Cl)C>C(Cl)(Cl)Cl.O>[Cl:19][CH2:18][CH2:17][CH:16]([OH:20])[CH2:15][O:11][C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

Participants

7

Conditions

Temperature
65 °C

Procedure

To a mixture of 1 mole (147 g.) of 1-naphthol, 350 ml. of water and 2 moles (112 g.) of potassium hydroxide was added at 54° C. 1 mole (143 g.) of 1,4-dichloro-2-butanol. The temperature of the reaction mixture was kept below 60° C. during the addition of the chlorobutanol. The reaction mixture was heated at 65° C. for 12 hr., then mixed with 500 ml. of water and 350 ml. of chloroform. The chloroform layer was separated, washed with water, dried over sodium sulfate, concentrated and the residual oil distilled under reduced pressure to give 128 g. of a crystalline solid which was distilled at 162°-165° C./0.01 mm. The solid was recrystallized with ether and pet. ether (30°-60°) to give material melting at 75°-77° C.

Workup

  1. addition, then mixed with 500 ml
  2. customThe chloroform layer was separated
  3. washwashed with water
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. distillationthe residual oil distilled under reduced pressure
  7. customto give 128 g
  8. distillationof a crystalline solid which was distilled at 162°-165° C./0.01 mm
  9. customThe solid was recrystallized with ether and pet. ether (30°-60°)

Sources & evidence

ORD record
ord-aa64a9d4b32f41809b0b82ea837fb5f8
Source dataset
uspto-grants-1986_09
Patent number
US04609735

Linked notes

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