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2,4-anhydro-3,5-bis-O-(phenylmethyl)-D-lyxonic acid methyl ester → HCID 15725611, 화합물

HRID 1450361
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HRID 1450361 반응식
[CH3:1][O:2][C:3]([C@H:5]1[O:16][C@H:15]([CH2:17][O:18]CC2C=CC=CC=2)[C@@H:6]1[O:7]CC1C=CC=CC=1)=[O:4].[H][H]>[OH-].[OH-].[Pd+2].CO>[CH3:1][O:2][C:3]([C@H:5]1[O:16][C@H:15]([CH2:17][OH:18])[C@@H:6]1[OH:7])=[O:4]
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참가 물질

5

반응물 2

HCID 147595602,4-anhydro-3,5-bis-O-(phenylmethyl)-D-lyxonic acid methyl esterHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 15725611HCID 15725611, 화합물수율 96.2%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

실험 절차

A slurry of 1.01 g of 2,4-anhydro-3,5-bis-O-(phenylmethyl)-D-lyxonic acid methyl ester (prepared by the procedure in Tetrahedron Letters, Vol 31, No. 33, p4787, 1990), 0.253 g of palladium hydroxide on carbon, and 30 ml of methyl alcohol is hydrogenated under a balloon of hydrogen (1 atm.) for 2.5 hours. The mixture is filtered through diatomaceous earth, washed with ethyl acetate and ethyl alcohol, and concentrated in vacuo to give 0.460 g of the desired product.

후처리

  1. filtrationThe mixture is filtered through diatomaceous earth
  2. washwashed with ethyl acetate and ethyl alcohol
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-29a33b99a75040c3b4c5868a708ae4db
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05602118

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