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4-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)benzoic acid → 4-(1,4-Dioxaspiro[4.5]decan-8-yl)benzoic acid

HRID 1809887
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HRID 1809887 반응식
[O:1]1[C:5]2([CH2:10][CH2:9][C:8]([C:11]3[CH:19]=[CH:18][C:14]([C:15]([OH:17])=[O:16])=[CH:13][CH:12]=3)=[CH:7][CH2:6]2)[O:4][CH2:3][CH2:2]1>CO.[Pd]>[O:1]1[C:5]2([CH2:10][CH2:9][CH:8]([C:11]3[CH:12]=[CH:13][C:14]([C:15]([OH:17])=[O:16])=[CH:18][CH:19]=3)[CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 595560954-(1,4-Dioxaspiro[4.5]dec-7-en-8-yl)benzoic acid

생성물 1

HCID 299215764-(1,4-Dioxaspiro[4.5]decan-8-yl)benzoic acid수율 97.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 5.3 g of 4-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)benzoic acid in 30 mL of methanol was added 2.3 g of Pd/C (10% wt). The suspension was stirred under H2 (balloon) for 1 h, filtered through celite pad and concentrated to dryness to give the desired product (5.2 g, yield: 97%) as a white solid: 1H NMR (CDCl3) δ 8.06-8.01 (2H, m), 7.58-7.53 (2H, m), 4.02 (4H, s), 2.73-2.67 (2H, m), 2.70-2.61 (1H, m), 1.93-1.64 (8H, m); MS: 262 (M+1)+.

후처리

  1. filtrationfiltered through celite pad
  2. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-0c56841ec50d4b61a12af429ac2f112e
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08362003B2

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