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Hydrochloric Acid → 6-(2,2-difluoroethoxy)nicotinic acid

HRID 341551
ノート
印刷プレビュー

反応式

HRID 341551 の反応式
[OH-].[K+].Cl[C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[CH:6][N:5]=1.[F:13][CH:14]([F:17])[CH2:15][OH:16].Cl>CS(C)=O.O>[F:13][CH:14]([F:17])[CH2:15][O:16][C:4]1[N:5]=[CH:6][C:7]([C:8]([OH:10])=[O:9])=[CH:11][CH:12]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 14797Potassium Hydroxide2 回HCID 792226-Chloronicotinic acidHCID 1361872,2-Difluoroethan-1-ol2 回

生成物 1

HCID 251162916-(2,2-difluoroethoxy)nicotinic acid収率 96.3%

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide
溶媒
HCID 962Water溶媒

実験手順

Powdered potassium hydroxide (712 mg, 12.7 mmol) was added to a mixture of 6-chloronicotinic acid (500 mg, 3.17 mmol) and 2,2-difluoroethanol (520 mg, 6.35 mmol) in DMSO (15 mL) and the mixture was stirred at 120 C for 14 h. An additional two equivalents of 2,2-difluoroethanol and potassium hydroxide were added and the mixture was heated for 24 h. The mixture was cooled to room temperature, diluted with water (5 mL), acidified with 1N aq. HCl (to pH 1) and extracted with EtOAc (3×50 mL). The combined organic layers were washed with water (2×25 mL) then brine (50 mL) and concentrated under reduced pressure to provide title compound as a beige solid (620 mg, 96%). Method B HPLC-MS: MH+ requires m/z=204. Found: m/z=204, Rt=1.54 min (90%).

後処理

  1. temperaturethe mixture was heated for 24 h
  2. extractionextracted with EtOAc (3×50 mL)
  3. washThe combined organic layers were washed with water (2×25 mL)
  4. concentrationbrine (50 mL) and concentrated under reduced pressure

出典と根拠

ORDレコード
ord-2b7768f1002f4dd59f20f18a65f7dd7b
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895733B2

反応ノート

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