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Ammonium Chloride → Methyl 3-chloro-5-(hydroxymethyl)benzoate

HRID 1656476
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HRID 1656476 반응식
[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:12]=[C:11]([Cl:13])[CH:10]=[C:6]([C:7](O)=[O:8])[CH:5]=1.[Cl-].[NH4+]>O1CCCC1>[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:5]=[C:6]([CH2:7][OH:8])[CH:10]=[C:11]([Cl:13])[CH:12]=1
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참가 물질

4

반응물 2

HCID 25517Ammonium ChlorideHCID 247289213-Chloro-5-(methoxycarbonyl)benzoic acid

생성물 1

HCID 53712641Methyl 3-chloro-5-(hydroxymethyl)benzoate수율 107%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In a 3 liter 3-necked round-bottom flask equipped with mechanical stirrer and nitrogen inlet was placed 5-chloroisophthalic acid monomethyl ester (29.4 g). Borane tetrahydrofuran complex in tetrahydrofuran solution (1M, 280 ml) was then added to the flask dropwise at room temperature. The resulting solution was stirred at room temperature overnight. The reaction mixture was poured into saturated aqueous ammonium chloride solution (750 ml) and extracted with ethyl acetate (3×500 ml). The combined organic layers were agitated with 2% aqueous hydrochloric acid, washed with water, dried and the solvent eliminated in the rotavap yielding 29.4 g of 3-chloro-5-hydroxymethyl benzoic acid methyl ester as a clear oil.

후처리

  1. customIn a 3 liter 3-necked round-bottom flask equipped with mechanical stirrer and nitrogen inlet
  2. extractionextracted with ethyl acetate (3×500 ml)
  3. stirringThe combined organic layers were agitated with 2% aqueous hydrochloric acid
  4. washwashed with water
  5. customdried

출처 및 근거

ORD 기록
ord-48dfb1432a1341d8bf07d6725611ace2
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05254584

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