Trifluoroacetic acid → 2-[4-(Methoxycarbonyl)oxan-4-yl]acetic acid

HRID 9534

반응식

HRID 9534 반응식
C([O:5][C:6](=[O:18])[CH2:7][C:8]1([C:14]([O:16][CH3:17])=[O:15])[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1)(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[CH3:17][O:16][C:14]([C:8]1([CH2:7][C:6]([OH:18])=[O:5])[CH2:9][CH2:10][O:11][CH2:12][CH2:13]1)=[O:15]

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 21985691methyl 4-(2-tert-butoxy-2-oxoethyl)tetrahydro-2H-pyran-4-carboxylate

생성물 1

HCID 219856952-[4-(Methoxycarbonyl)oxan-4-yl]acetic acid수율 104.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of methyl 4-(2-tert-butoxy-2-oxoethyl)tetrahydro-2H-pyran-4-carboxylate (1.1 g, 4.26 mmol) in dichloromethane (5.0 mL) was added trifluoroacetic acid (5.0 mL) and the resulting solution was stirred at rt for 5 h. The mixture was concentrated under reduced pressure to afford [4-(methoxycarbonyl)tetrahydro-2H-pyran-4-yl]acetic acid (900 mg, 94%), which was used in the next step without further purification. LC-MS ret. time 0.93 min, m/z 202.9 (MH+); 1H NMR (300 MHz, DMSO-d6) δ 1.60–1.70 (m, 2H), 2.10–2.15 (m, 2H), 2.68 (s, 2H), 3.62–3.71 (m, 2H), 3.72 (s, 3), 3.79–3.86 (m, 2H).

후처리

  1. concentrationThe mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-32f0b45fdb2849eb997c167048a03d3c
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091228B2

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