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Hydrochloric Acid → 2-(2-Benzyloxy-5-chlorophenyl)cyclopentene-1-boronic Acid

HRID 1767210
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HRID 1767210 반응식
C([Li])CCC.Br[C:7]1[CH2:11][CH2:10][CH2:9][C:8]=1[C:12]1[CH:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:13]=1[O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[B:27](OC(C)C)([O:32]C(C)C)[O:28]C(C)C.Cl>O1CCCC1.CCOCC>[CH2:20]([O:19][C:13]1[CH:14]=[CH:15][C:16]([Cl:18])=[CH:17][C:12]=1[C:8]1[CH2:9][CH2:10][CH2:11][C:7]=1[B:27]([OH:32])[OH:28])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 211129001-Bromo-2-(2-benzyloxy-5-chlorophenyl)cyclopenteneHCID 178418339Butyllithium

생성물 1

HCID 211129122-(2-Benzyloxy-5-chlorophenyl)cyclopentene-1-boronic Acid수율 58%

시약·촉매·용매 2

HCID 3283
Diethyl Ether
용매
HCID 8028Tetrahydrofuran용매

실험 절차

A solution of n-butyllithium (0.73 ml, 1.6M in hexanes, 1.17 mmol) was added to a solution of 1-bromo-2-(2-benzyloxy-5-chlorophenyl)cyclopentene (424 mg, 1.17 mmol) in anhydrous tetrahydrofuran (12 ml) at −78° C. under nitrogen. The resulting solution was stirred for 15 minutes and triisopropyl borate (440 mg, 2.34 mmol) was added. The mixture was allowed to warm to room temperature, 1M hydrochloric acid (20 ml) was added and stirred vigorously for 15 minutes. After diluting with ether the organic phase was dried (magnesium sulphate), evaporated and purified by chromatography on silica (1:4 ethyl acetate/iso-hexane) to give the title compound as a white solid (214 mg, 58%). LC/MS: Rt 3.4, [2 MH−] 637.3.

후처리

  1. stirringstirred vigorously for 15 minutes
  2. dry with materialwas dried (magnesium sulphate)
  3. customevaporated
  4. custompurified by chromatography on silica (1:4 ethyl acetate/iso-hexane)

출처 및 근거

ORD 기록
ord-42cf77559e0e4c269ab81e6672b945c7
출처 데이터셋
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07232821B2

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