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

HRID 2419896
ノート
印刷プレビュー

反応式

HRID 2419896 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 13384252Methyl 6-chloro-2-naphthoate

生成物 1

HCID 13384253(6-Chloronaphthalen-2-yl)methanol収率 98%

試薬・触媒・溶媒 2

HCID 241Benzene溶媒HCID 3283Diethyl Ether溶媒3 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-2cc89c1d62a44c6980fb0dd0bc2023fd
出典データセット
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04107329

反応ノート

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