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Trifluoroacetic acid → 2-Nitrophenol

HRID 1949614
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반응식

HRID 1949614 반응식
C(O)(C(F)(F)F)=[O:2].C(O[C@@H](CCNC(OCC1C=CC=CC=1)=O)C(=O)[O:19][C:20]1[C:25](F)=[C:24](F)[C:23](F)=[C:22](F)[C:21]=1F)(=O)C1C=CC=CC=1.[NH4+:45].[OH-:46]>O>[N+:45]([C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=1[OH:19])([O-:2])=[O:46]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 14923Ammonium HydroxideHCID 58503143(S)-4-(benzyloxycarbonylamino)-1-oxo-1-(perfluorophenoxy)butan-2-yl benzoate

생성물 1

HCID 69472-Nitrophenol수율 40%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To a stirring solution of TFA (1 mL) and water (0.2 mL) at 0° C. was added 3′,4′,3′″,4′″-tetra-deoxy-1-(N-Boc-2(S)-hydroxy-3-amino-propionyl)-neomycin (3, 0.164 mmol) and the reaction was stirred for 30 minutes, and checked for completeness by MS. Upon completion, the reaction was diluted with water (10 mL) and lyophilized to yield a crude, which was dissolved in conc. NH4OH (1.5 mL) and purified on a 1-inch reverse-phase HPLC column (0-10% ACN, 10 mM NH4OH) to yield 3′,4′,3′″,4′″-tetra-deoxy-1-(2(S)-hydroxy-3-amino-propionyl)-neomycin (4, 48.7 mg, 0.076 mmol, 40% yield): MS: m/z (M+H)+ calc. 638.0, obs.: 638.2; CLND 99.6% purity.

후처리

  1. customto yield a crude, which
  2. custompurified on a 1-inch reverse-phase HPLC column (0-10% ACN, 10 mM NH4OH)

출처 및 근거

ORD 기록
ord-fae8b37284df451488d315b094ecafcd
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399419B2

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