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Hydrochloric Acid → 10-Chloro-1-anthracenemethanol

HRID 1381797
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반응식

HRID 1381797 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 1337541110-Chloro-1-anthracenemethanol수율 81.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-507b94d5dc264582beec162ef0312b8b
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04803221

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