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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Hydrochloric Acid → (3,5-Dibromophenyl)methanol

HRID 725030
ノート
印刷プレビュー

反応式

HRID 725030 の反応式
[BH4-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([Br:12])[CH:11]=1)[CH:7]=[O:8].Cl>CO>[Br:3][C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([Br:12])[CH:11]=1)[CH2:7][OH:8]
参加物反応条件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 6220773,5-DibromobenzaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 7009423(3,5-Dibromophenyl)methanol収率 94.9%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

Sodium borohydride (0.75 g) was added portionwise to a stirred suspension of 3,5-dibromobenzaldehyde (10.46 g) in methanol (50 ml) at 0° C. The mixture was stirred at 0° C. for 30 minutes, allowed to warm to room temperature and then its pH was adjusted to 2 using concentrated hydrochloric acid. Evaporation under vacuum provided a residue which was partitioned between ethyl acetate and water. The organic phase was washed with water, dried(MgSO4), then evaporated under vacuum to furnish the title compound as a solid (10.0 g), m.p. 103°-104° C. Found: C, 31.98; H, 2.23. C7H6Br2O requires C, 31.61; H, 2.77%.

後処理

  1. temperatureto warm to room temperature
  2. customEvaporation under vacuum
  3. customprovided a residue which
  4. customwas partitioned between ethyl acetate and water
  5. washThe organic phase was washed with water, dried(MgSO4)
  6. customevaporated under vacuum

出典と根拠

ORDレコード
ord-6a31763ce7e5436b85040d5a4941718f
出典データセット
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05705523

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート