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p-Toluenesulfonic acid monohydrate → HCID 86706149, 화합물

HRID 2176302
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HRID 2176302 반응식
[C:1]([O:5][C:6]([C:8]1([CH:16]=[CH2:17])[CH2:13][O:12]C(C)(C)[O:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[C:1]([O:5][C:6](=[O:7])[C:8]([CH2:13][OH:12])([CH2:9][OH:10])[CH:16]=[CH2:17])([CH3:4])([CH3:2])[CH3:3]
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참가 물질

4

반응물 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 86706150HCID 86706150, 화합물

생성물 1

HCID 86706149HCID 86706149, 화합물수율 82%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 2,2-dimethyl-5-vinyl-[1,3]dioxane-5-carboxylic acid tert-butyl ester (969 mg, 4 mmol) and 4-toluenesulfonic acid hydrate (76 mg, 0.4 mmol) in methanol (10 mL) was stirred at room temperature for 30 min. The solvent was evaporated and the residue was purified by silica gel chromatography using a gradient of iso-hexanes/ethyl acetate 4:1 to 1:1 to afford the title compound (660 mg, 82%) as a white solid. 1H NMR (300 MHz, d6-DMSO): δ 1.38 (s, 9H), 3.54-3.68 (m, 4H), 4.56 (t, J=5.4 Hz, 2H), 5.12 (d, J=10.5 Hz, 1H), 5.14 (d, J=18.3 Hz, 1H), 5.80 (dd, J=18.3, 10.5 Hz, 1H). LCMS (m/z) 225.2 [M+Na], Tr=1.47 min.

후처리

  1. customThe solvent was evaporated
  2. customthe residue was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-b869d30b96f84cc68d7d53d8fbaaac88
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062092B2

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