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Water → 1,2-dibenzyl 1-tert.butyl 1-(formylmethyl)-4-methyl-1,1,2(R)-pentanetricarboxylate

HRID 1464362
ノート
印刷プレビュー

反応式

HRID 1464362 の反応式
[CH3:1][CH:2]([CH3:36])[CH2:3][C@@H:4]([C:26]([O:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)=[O:27])[C:5]([CH2:23][CH:24]=C)([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[C:6]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:7].I([O-])(=O)(=O)=O.[Na+].C(OCC)C.[OH2:48]>[Os](=O)(=O)(=O)=O>[CH:24]([CH2:23][C:5]([C:16]([O:18][C:19]([CH3:22])([CH3:20])[CH3:21])=[O:17])([C:6]([O:8][CH2:9][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)=[O:7])[C@H:4]([C:26]([O:28][CH2:29][C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)=[O:27])[CH2:3][CH:2]([CH3:36])[CH3:1])=[O:48]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 3283Diethyl EtherHCID 23667635Sodium periodate2 回HCID 678262121,2-dibenzyl 1-tert.butyl 4-methyl-1-(prop-2-en-1yl)-1,1,2(R)-pentanetricarboxylate

生成物 1

HCID 867477791,2-dibenzyl 1-tert.butyl 1-(formylmethyl)-4-methyl-1,1,2(R)-pentanetricarboxylate

試薬・触媒・溶媒 1

HCID 30318
Osmium Tetroxide
触媒

実験手順

A mixture of 1.23 g of 1,2-dibenzyl 1-tert.butyl 4-methyl-1-(prop-2-en-1yl)-1,1,2(R)-pentanetricarboxylate, 3 ml of a 1% aqueous solution of osmium tetroxide, 2.44 g of sodium periodate, 15 ml of diethyl ether and 15 ml of water was stirred at room temperature for 1 hour. A further 3.25 g of sodium periodate were added and the mixture was stirred at room temperature for 24 hours. The ether layer was separated and the aqueous layer was extracted with diethyl ether. The combined ether layers were washed repeatedly with 5% aqueous ascorbic acid solution and saturated sodium chloride solution. After drying over magnesium sulfate, the solution was evaporated and the residue was purified by flash chromatography on silica gel using hexane/diethyl ether (8:1) for the elution. There was obtained 0.955 g of 1,2-dibenzyl 1-tert.butyl 1-(formylmethyl)-4-methyl-1,1,2(R)-pentanetricarboxylate in the form of a colorless oil; MS: 497 (M+H)+.

後処理

  1. stirringthe mixture was stirred at room temperature for 24 hours
  2. customThe ether layer was separated
  3. extractionthe aqueous layer was extracted with diethyl ether
  4. washThe combined ether layers were washed repeatedly with 5% aqueous ascorbic acid solution and saturated sodium chloride solution
  5. dry with materialAfter drying over magnesium sulfate
  6. customthe solution was evaporated
  7. customthe residue was purified by flash chromatography on silica gel
  8. washfor the elution

出典と根拠

ORDレコード
ord-d6f70bcbcb2d4c6aa5bd7cb36d6fed18
出典データセット
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05304549

反応ノート

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