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Trimethyl borate → Boronic acid, (4-ethylphenyl)-

HRID 232750
ノート
印刷プレビュー

反応式

HRID 232750 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH3:9])=[CH:4][CH:3]=1.[Mg].[B:11](OC)([O:14]C)[O:12]C>CCOCC>[CH2:8]([C:5]1[CH:6]=[CH:7][C:2]([B:11]([OH:14])[OH:12])=[CH:3][CH:4]=1)[CH3:9]
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 8470Trimethyl borateHCID 153131-Bromo-4-ethylbenzeneHCID 5462224Magnesium2 回

生成物 1

HCID 2734352Boronic acid, (4-ethylphenyl)-収率 41%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒3 回

実験手順

A solution of 1-bromo-4-ethyl benzene (2.0 g, 11 mmol) in dry ether (5 ml) was added to magnesium turnings (311 mg, 13 mmol), which had been suspended in dry ether, by a dropwise addition. After addition was complete, the suspension was refluxed for a period of 15 min after which nearly all of the magnesium had reacted. This solution was then added to trimethy borate (1.12 g, 11 mmol) previously dissolved in ether (5 ml) at -78° C., the solution was warmed to room temperature and stirred for 90 min. The reaction was quenched by the addition of 10% aqueous HCl (2 ml) and the solution was extracted with ether. The combined ether extracts was extracted with 1M NaOH (2×20 ml), the aqueous extracts were acidified with dilute HCl to pH 2 and extracted with ether (2×25 ml). The combined ether extracts was washed once with water (10 ml), dried and evaporated to produce a white solid (676 mg, 38% yield), m.p. 138°-140° C.

後処理

  1. additionAfter addition
  2. customhad reacted
  3. customThe reaction was quenched by the addition of 10% aqueous HCl (2 ml)
  4. extractionthe solution was extracted with ether
  5. extractionThe combined ether extracts was extracted with 1M NaOH (2×20 ml)
  6. extractionextracted with ether (2×25 ml)
  7. washThe combined ether extracts was washed once with water (10 ml)
  8. customdried
  9. customevaporated

出典と根拠

ORDレコード
ord-c1c147a2cbeb4858ba5715228f5b065a
出典データセット
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05591761

反応ノート

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