Hydrochloric Acid → 2-Chloro-5-iodobenzyl alcohol

HRID 602057ノート

反応式

HRID 602057 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([I:11])=[CH:7][C:3]=1[C:4](O)=[O:5].C1(C)C=CC=CC=1.[H-].C([Al+]CC(C)C)C(C)C.Cl>CO>[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([I:11])=[CH:7][C:3]=1[CH2:4][OH:5]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 1140Toluene2 回HCID 5196382-Chloro-5-iodobenzoic acidHCID 21225700Diisobutylaluminumhydride

生成物 1

HCID 671539432-Chloro-5-iodobenzyl alcohol収率 34%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution of 2-chloro-5-iodobenzoic acid (28 g, 99 mmoles) and toluene (198 mL) was cooled to 0° C. A 1M diisobutyl aluminium hydride (DIBAL) solution in toluene 208 mL, 208 mmol) solution was added drop wise over 20 minutes. The solution was allowed to slowly warm to rt. After 16 h the solution was cooled to 0° C., MeOH and 1M HCl was slowly added (exothermic reaction). The solution became clumpy and was filtered and the clumps washed with EtOAc. The organic phase was then isolated and the aqueous layer washed with EtOAc. The combined organic extracts were then washed with brine, dried (Na2SO4), and concentrated. The product was purified by Biotage chromatography (0%-100% EtOAc/Hexanes) to afford 9.01 g of product as a solid (34%). 1H NMR (400 MHz, chloroform-d) δ ppm 7.85 (d, J=2.02 Hz, 1 H) 7.55 (dd, J=8.34, 2.27 Hz, 1 H) 7.09 (d, J=8.34 Hz, 1 H) 4.74 (s, 2 H) 2.25 (s, 1 H).

後処理

  1. temperatureAfter 16 h the solution was cooled to 0° C.
  2. custom(exothermic reaction)
  3. filtrationwas filtered
  4. washthe clumps washed with EtOAc
  5. customThe organic phase was then isolated
  6. washthe aqueous layer washed with EtOAc
  7. washThe combined organic extracts were then washed with brine
  8. dry with materialdried (Na2SO4)
  9. concentrationconcentrated
  10. customThe product was purified by Biotage chromatography (0%-100% EtOAc/Hexanes)

出典と根拠

ORDレコード
ord-ac638998e7b84954894bb41248054734
出典データセット
uspto-grants-2011_03
特許番号
US07902394B2

反応ノート

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