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Hydrochloric Acid → 4-(3-Hydroxyoxetan-3-yl)benzoic acid

HRID 72977
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HRID 72977 반응식
BrC1C=CC(C(O)=O)=CC=1.C([Li])CCC.O1CC(=O)C1.Cl.[OH:22][C:23]1([C:27]2[CH:35]=[CH:34][C:30]([C:31]([OH:33])=[O:32])=[CH:29][CH:28]=2)[CH2:26][O:25][CH2:24]1.C(O)(=O)C1C=CC=CC=1>C1COCC1.C(OCC)(=O)C>[OH:22][C:23]1([C:27]2[CH:28]=[CH:29][C:30]([C:31]([OH:33])=[O:32])=[CH:34][CH:35]=2)[CH2:26][O:25][CH2:24]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 313Hydrochloric AcidHCID 114644-Bromobenzoic acidHCID 150242543-OxetanoneHCID 866724754-(3-Hydroxyoxetan-3-yl)benzoic acid benzoic acidHCID 178418339Butyllithium

생성물 1

HCID 682916814-(3-Hydroxyoxetan-3-yl)benzoic acid

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
2회
HCID 8857Ethyl Acetate용매

실험 절차

To 4-bromobenzoic acid (434 mg, 2.16 mmol) in THF (9 mL) at −78° C. was added dropwise n-butyllithium (2.84 mL of 1.6 M in hexanes, 4.54 mmol). The reaction mixture was stirred for 30 minutes, then oxetan-3-one (218 mg, 3.03 mmol) in THF (1 mL) was added dropwise. The reaction mixture was stirred for 30 minutes at −78° C. and allowed to warm to room temperature over 30 minutes. The reaction mixture was diluted with ethyl acetate (15 mL) and acidified to pH 2 with 2 N HCl. The layers were separated and the aqueous was re-extracted with ethyl acetate (15 mL). The combined organics were washed with brine solution (10 mL), dried over MgSO4 and concentrated in vacuo to give a white solid as a 1:1 mixture of 4-(3-hydroxyoxetan-3-yl)benzoic acid/benzoic acid (380 mg, 91%).

후처리

  1. stirringThe reaction mixture was stirred for 30 minutes at −78° C.
  2. customThe layers were separated
  3. extractionthe aqueous was re-extracted with ethyl acetate (15 mL)
  4. washThe combined organics were washed with brine solution (10 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customto give a white solid

출처 및 근거

ORD 기록
ord-4cd6ef90f71d4dc68992b3443b607049
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08828996B2

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