Hydrochloric Acid → 3-Bromo-5-(hydroxymethyl)benzoic acid

HRID 14101

반응식

HRID 14101 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([C:11]([O:13]C)=[O:12])[CH:10]=1)[C:5](O)=[O:6].[BH4-].[Li+].C(O)C.Cl>O1CCCC1>[Br:1][C:2]1[CH:10]=[C:9]([CH:8]=[C:4]([CH2:5][OH:6])[CH:3]=1)[C:11]([OH:13])=[O:12]

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 4148881Lithium borohydrideHCID 225936413-Bromo-5-(methoxycarbonyl)benzoic acid

생성물 1

HCID 81671273-Bromo-5-(hydroxymethyl)benzoic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To an ice-cold solution of 3-bromo-5-(methoxycarbonyl)benzoic acid prepared by the method in Preparation 2 (10.3 g, 40 mmol) in anhydrous tetrahydrofuran (100 mL) is added lithium borohydride (12 g, 550 mmol) portion-wise. The reaction is stirred 4 h at this temperature. Absolute ethanol (20 mL) is added dropwise, and the reaction is stirred 1.5 h. The reaction is slowly poured on ice, and 10% hydrochloric acid (aq) is added until gas evolution ceased. The aqueous layer is extracted with chloroform, and the organic layer is washed with brine, dried (magnesium sulfate), filtered, and concentrated under reduced pressure to give the title compound. ESI MS m/z 229, 231 [M−H]−.

후처리

  1. stirringthe reaction is stirred 1.5 h
  2. additionis added until gas evolution
  3. extractionThe aqueous layer is extracted with chloroform
  4. washthe organic layer is washed with brine
  5. dry with materialdried (magnesium sulfate)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-479f562303ec43e8b64ace9bb92a85a5
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07727997B2

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