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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trimethyl borate → 2-Fluoro-3-iodobenzyl alcohol

HRID 2096972
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HRID 2096972 반응식
B(OC)(OC)OC.[F:8][C:9]1[C:17]([I:18])=[CH:16][CH:15]=[CH:14][C:10]=1[C:11](O)=[O:12]>O1CCCC1>[F:8][C:9]1[C:17]([I:18])=[CH:16][CH:15]=[CH:14][C:10]=1[CH2:11][OH:12]
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참가 물질

4

반응물 2

HCID 8470Trimethyl borateHCID 110545892-Fluoro-3-iodobenzoic acid

생성물 1

HCID 120412982-Fluoro-3-iodobenzyl alcohol수율 97%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Trimethyl borate (1.92 mL, 17.2 mmol) was added dropwise to a stirred solution of 2-fluoro-3-iodobenzoic acid (preparation 22b, 4.39 g, 16.5 mmol) in tetrahydrofuran (25 mL) at 0° C. and the mixture was stirred for a further 15 minutes at this temperature. Then borane-methyl sulfide complex (10 M, 4.4 mL, 44 mmol) in tetrahydrofuran (3 mL) was added dropwise to the mixture at 0° C. and the mixture was then allowed to warm to room temperature. After 1 hour, the mixture was carefully quenched by dropwise addition of methanol (10 mL). After stirring overnight, the mixture was concentrated in vacuo and ethyl acetate was added to the residue. The organic layer was washed with saturated aqueous potassium carbonate solution, brine, dried (MgSO4) and evaporated to give the title compound (4.03 g, 97%) as an oil.

후처리

  1. waitAfter 1 hour
  2. customthe mixture was carefully quenched by dropwise addition of methanol (10 mL)
  3. stirringAfter stirring overnight
  4. concentrationthe mixture was concentrated in vacuo and ethyl acetate
  5. additionwas added to the residue
  6. washThe organic layer was washed with saturated aqueous potassium carbonate solution, brine
  7. dry with materialdried (MgSO4)
  8. customevaporated

출처 및 근거

ORD 기록
ord-a3299156cbdd4da2b0436335fbd7808c
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450341B2

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