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Hydrochloric Acid → 10-Chloro-1-anthracenemethanol

HRID 1381797
ノート
印刷プレビュー

反応式

HRID 1381797 の反応式
[Cl:1][C:2]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[C:16](OCC)=[O:17].[Li+].[BH4-].Cl>C1COCC1>[Cl:1][C:2]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[CH2:16][OH:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 4148881Lithium borohydrideHCID 21276219Ethyl 10-chloroanthracene-1-carboxylate

生成物 1

HCID 1337541110-Chloro-1-anthracenemethanol収率 81.6%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of ethyl 10-chloroanthracene-1-carboxylate (37B, 14.86 g, 0.052 mol) in THF (300 mL) was treated with LiBH4 (Alfa, 1.14 g, 0.052 mol) and refluxed for 16 h. The reaction mixture was poured into ice water and acidified with conc. HCl to pH=2. The solid was filtered, washed with H2O (500 mL), air dried and then chromatographed on a plug of SiO2 (500 g) using EtOAc as the eluting solvent. The solvent was removed by rotary evaporation to give a solid, which was crystallized from CCl4 to give 10.3 g (81%) of 10-chloro-1-anthracenemethanol mp 138°-140°, (C, H, Cl).

後処理

  1. temperaturerefluxed for 16 h
  2. filtrationThe solid was filtered
  3. washwashed with H2O (500 mL), air
  4. customdried
  5. customchromatographed on a plug of SiO2 (500 g)
  6. customThe solvent was removed by rotary evaporation
  7. customto give a solid, which
  8. customwas crystallized from CCl4

出典と根拠

ORDレコード
ord-507b94d5dc264582beec162ef0312b8b
出典データセット
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04803221

反応ノート

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