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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonium Chloride → (3-Benzyloxy-4-iodophenyl)methanol

HRID 1361091
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HRID 1361091 반응식
C([C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][C:17]=1[I:18])[C:11]([O:13]C)=O)C1C=CC=CC=1.[BH4-].[Li+].[Cl-].[NH4+]>O1CCCC1>[CH2:11]([O:13][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][C:17]=1[I:18])[CH2:11][OH:13])[C:10]1[CH:15]=[CH:16][CH:17]=[CH:8][CH:9]=1
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참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 4148881Lithium borohydrideHCID 66971745Methyl 3-benzyl-4-iodobenzoate

생성물 1

HCID 45140291(3-Benzyloxy-4-iodophenyl)methanol수율 196.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 139 g (374 mmol) of methyl 3-benzyl-4-iodobenzoate in 550 ml of tetrahydrofuran is added dropwise to a solution of 12.9 g (563 mmol) of lithium borohydride in 150 ml of tetrahydrofuran and the reaction medium is then refluxed for 3 hours. After cooling, 300 ml of saturated aqueous ammonium chloride solution are added and the reaction medium is extracted with ethyl acetate. The organic phase is washed with water, dried over sodium sulfate, filtered and evaporated. 125 g (97%) of 3-benzyloxy-4-iodobenzyl alcohol are obtained in the form of white crystals.

후처리

  1. temperaturethe reaction medium is then refluxed for 3 hours
  2. temperatureAfter cooling
  3. extractionthe reaction medium is extracted with ethyl acetate
  4. washThe organic phase is washed with water
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-70c3c4ba0568430fb9ece1e61242a220
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879907B2

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