Hydrochloric Acid → (6-Chloronaphthalen-2-yl)methanol

HRID 2419896Notes

Reaction equation

HRID 2419896 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12](OC)=[O:13])[CH:6]=[CH:5]2.Cl.O>CCOCC.C1C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([CH2:12][OH:13])[CH:6]=[CH:5]2

Participants

6

Procedure

A solution of the methyl 6-chloro-2-naphthoate (111 g.) in ether (2.5 1.) is added, dropwise below 25° C. under nitrogen, to a stirred mixture of ether (250 ml.) and a 70% solution (250 ml.) of sodium dihydro-bis-(2-methoxyethoxy)aluminate in benzene during 1 hour. The mixture is stirred for a further 30 minutes and 2N-hydrochloric acid (250 ml.) is added cautiously. The solution is decanted from undissolved solid, and concentrated hydrochloric acid is added to the solid until it dissolves. The two solution thus obtained are combined, and ether (1 l.) and a mixture of ice and water (1 l.) are added. The ethereal layer is separated, and the aqueous phase extracted with ether. The ethereal solutions are combined, washed with water, dried and evaporated to give 6-chloro-2-hydroxymethylnaphthalene (95 g.) which may be further purified by crystallisation from toluene to give material of m.p. 134°-137° C.

Workup

  1. customThe solution is decanted from undissolved solid, and concentrated hydrochloric acid
  2. additionis added to the solid until it
  3. dissolutiondissolves
  4. customThe two solution thus obtained
  5. additionare added
  6. customThe ethereal layer is separated
  7. extractionthe aqueous phase extracted with ether
  8. washwashed with water
  9. customdried
  10. customevaporated

Sources & evidence

ORD record
ord-2cc89c1d62a44c6980fb0dd0bc2023fd
Source dataset
uspto-grants-1978_08
Patent number
US04107329

Reaction notes

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