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Methyl Isocyanate → 1-Hexadecylthio-2-methylcarbamoyloxy-3-trityloxypropane

HRID 728440
ノート
印刷プレビュー

反応式

HRID 728440 の反応式
[CH2:1]([S:17][CH2:18][CH:19]([OH:41])[CH2:20][O:21][C:22]([C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[CH3:42][N:43]=[C:44]=[O:45]>ClCCl.CN(C)C1C=CN=CC=1>[CH2:1]([S:17][CH2:18][CH:19]([O:41][C:44](=[O:45])[NH:43][CH3:42])[CH2:20][O:21][C:22]([C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)([C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1)[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 12228Methyl IsocyanateHCID 130028641-Hexadecylthio-3-trityloxy-2-propanol

生成物 1

HCID 198842011-Hexadecylthio-2-methylcarbamoyloxy-3-trityloxypropane

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane溶媒

実験手順

To a solution of 1-hexadecylthio-3-trityloxy-2-propanol c1 4.6 g (8.0 mmol) in dichloromethane 100 ml are added 4-dimethylaminopyridine 1.17 g (9.6 mmol) and methyl isocyanate 4.72 ml (80 mmol). The solution is allowed to stand at room temperature for 72 hr and concentrated. The residue is chromatographed on SiO2 (46 g) and eluted with ethyl acetate:hexane (1:5) to give 1-hexadecylthio-2-methylcarbamoyloxy-3-trityloxypropane c2 as a crude oil (5.6 g). The oil is dissolved in dichloromethane 100 ml and boron trifluoride-methanol complex 1.68 ml (15.5 mmol) is added under cooling. The resulting yellow solution is stirred at 0° C. for 15 min and then at room temperature for 1 hr. Sodium carbonate aq solution is added to neutralize the reaction mixture and an organic layer is separated. The organic layer is subjected to SiO2 (80 g) column chromatography and eluted with ethyl acetate:hexane (1:1) to afford crude crystals 2.07 g. The crystals are triturated and washed with pentane to yield the titled compound Vc1 1.205 g. The mother liqour is purified by Lobar column chromatography with the same solvent as described above to give additional Vc1 0.321 g (49% total yield), mp. 53°-55° C.

後処理

  1. concentrationconcentrated
  2. customThe residue is chromatographed on SiO2 (46 g)
  3. washeluted with ethyl acetate:hexane (1:5)

出典と根拠

ORDレコード
ord-729dcf45717941039d60a99ac19757a4
出典データセット
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05047540

反応ノート

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