Dimethyl dicarbonate → rel-Methyl (1R,2S)-3-oxo-2-pentylcyclopentaneacetate

HRID 2376

反応式

HRID 2376 の反応式
[O:1]=[C:2]1[CH2:6][CH2:5][C@@H:4]([CH2:7][C:8]([OH:10])=[O:9])[C@H:3]1[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[C:16](OC(OC)=O)(OC)=O>CO>[O:1]=[C:2]1[CH2:6][CH2:5][C@@H:4]([CH2:7][C:8]([O:10][CH3:16])=[O:9])[C@H:3]1[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]

参加物

4

反応物 2

HCID 3086Dimethyl dicarbonateHCID 16061083(1S,2R)-3-oxo-2-pentyl-cyclopentaneacetic acid

生成物 1

HCID 1738127rel-Methyl (1R,2S)-3-oxo-2-pentylcyclopentaneacetate収率 90%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

104 Mg (0.49 mmole) of (+)-cis-3-oxo-2-pentyl-1-cyclopentaneacetic acid (97:3 cis/trans ratio) in 0.5 ml of methanol were treated with 76 μl of dimethyl dicarbonate [CH3O(CO)O(CO)OCH3, origin: Bayer; 96 mg, 0.72 mmole, 1.5 eq.]. The resulting solution was heated to 45° during 16 h and then evaporated under vacuum. After distillation of the residue in a bulb-to-bulb apparatus (oven t. 150°/10 Pa), there were obtained 100 mg (0.44 mmole, yield 90%) of pure methyl (±)cis-3-oxo-2-pentyl-1-cyclopentaneacetate (97:3 cis/trans ratio).

後処理

  1. temperatureThe resulting solution was heated to 45° during 16 h
  2. customevaporated under vacuum
  3. distillationAfter distillation of the residue in a bulb-to-bulb apparatus (oven t. 150°/10 Pa)

出典と根拠

ORDレコード
ord-13f0bb09496b4e76add90df9bebc924b
出典データセット
uspto-grants-1998_03
特許番号
US05728866

関連ノート

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