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Cesium carbonate → 2-(2-Methoxycarbonylethylthio)ethyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl)-beta-D-galactopyranoside

HRID 653323
ノート
印刷プレビュー

反応式

HRID 653323 の反応式
[C:1]([O:4][C@@H:5]1[C@@H:14]([O:15][C:16](=[O:18])[CH3:17])[C@@H:13]([O:19][C@H:20]2[O:37][C@H:36]([CH2:38][O:39][C:40](=[O:42])[CH3:41])[C@H:31]([O:32][C:33](=[O:35])[CH3:34])[C@H:26]([O:27][C:28](=[O:30])[CH3:29])[C@H:21]2[O:22][C:23](=[O:25])[CH3:24])[C@@H:12]([CH2:43][O:44][C:45](=[O:47])[CH3:46])[O:11][C@H:6]1[O:7][CH2:8][CH2:9]Br)(=[O:3])[CH3:2].[SH:48][CH2:49][CH2:50][C:51]([O:53][CH3:54])=[O:52].C(=O)([O-])[O-].[Cs+].[Cs+].C(OCC)(=O)C.C(CC(C)(C)C)(C)C>[Cl-].C[N+](CCCCCCCC)(CCCCCCCC)CCCCCCCC.C1C=CC=CC=1.O>[C:1]([O:4][C@@H:5]1[C@@H:14]([O:15][C:16](=[O:18])[CH3:17])[C@@H:13]([O:19][C@H:20]2[O:37][C@H:36]([CH2:38][O:39][C:40](=[O:42])[CH3:41])[C@H:31]([O:32][C:33](=[O:35])[CH3:34])[C@H:26]([O:27][C:28](=[O:30])[CH3:29])[C@H:21]2[O:22][C:23](=[O:25])[CH3:24])[C@@H:12]([CH2:43][O:44][C:45](=[O:47])[CH3:46])[O:11][C@H:6]1[O:7][CH2:8][CH2:9][S:48][CH2:49][CH2:50][C:51]([O:53][CH3:54])=[O:52])(=[O:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 10796Cesium carbonateHCID 18050Methyl 3-mercaptopropionate2 回HCID 18516502EtOAc isooctaneHCID 228870902-Bromoethyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl)-beta-D-galactopyranoside

生成物 1

HCID 54172652
2-(2-Methoxycarbonylethylthio)ethyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl)-beta-D-galactopyranoside

試薬・触媒・溶媒 3

HCID 21218Trioctylmethylammonium chloride触媒HCID 241Benzene溶媒HCID 962Water溶媒

実験手順

2-Bromoethyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl)-β-D-galactopyranoside (15) (251 mg; 0.338 mmol), methyl 3-mercaptopropionate (38 μl; 0.35 mmol) methyltrioctylammonium chloride (ca 10 mg) and cesium carbonate (114 mg; 0.35 mmol) were dissolved in benzene (0.5 ml) and water (0.5 ml). The reaction mixture was stirred (magnet) over night and analyzed by TLC (SiO2, ethyl acetate:isooctane 4:1; reaction 2/3 completed). Methyl 3-mercaptopropionate (ca 20 μl) was added and the reaction mixture was stirred for 24 h (TLC showed complete reaction). The phases were separated, the water phase was extracted twice with methylene chloride and the combined organic phases were dried (sodium sulfate) which gave a yellow to green solution. Evaporation gave a syrup which was chromatographed (SiO2, ethyl acetate:isooctane 2:1) to give the title compound (22) as a syrup. Yield: 211 mg (80%). [α]D23 +70.0° (c 0.6; CHCl3); 1H-NMR (CDCl3, TMS) δ 5.57 (d, 1H, J3',4' =3.0 Hz, H4'), 5.39 (dd, 1H, J2',3' =11.0 Hz. H2'), 5.19 (dd, 1H, H3'), 5.17 (dd, 1H, J2,3 =11 Hz, H2), 5.00 (d, 1H, J1',2' =4.0 Hz, H1'), 4.80 (dd, 1H, J3,4 =3.0 Hz, H3), 4.51 (d, 1H, J1,2 =8.0 Hz, H1), 3.70 (s, 3H, CH3 --O), 2.82, 2.75, 2.63 (t, 2H each, J=7 Hz, CH2 --S, CH2 --CO), 2.13, 2.11, 2.08, 2.08, 2.06, 2.04, 1.98 (s, 3H each, CH3CO) ppm. 13C-NMR (CDCl3, TMS) δ 172.3 (COOCH3), 170.7, 170.6, 170.5, 170.4, 170.1, 169.8, 169.2 (CH3CO), 101.1 (Cl), 99.4 (Cl'), 77.1, 72.7, 72.0, 68.6, 68.5, 67.9, 67.4, 67.1 (C2-C5, C2'-C5'), 69.5 (OCH2), 62.0, 60.5 (C6, C6'), 51.8 (COOCH3), 34.7, 31.4, 27.4 (CH2S, CH2 --CO), 21.0, 20.7 (CH3CO) ppm.

後処理

  1. stirringthe reaction mixture was stirred for 24 h
  2. custom(TLC showed complete reaction)
  3. customThe phases were separated
  4. extractionthe water phase was extracted twice with methylene chloride
  5. dry with materialthe combined organic phases were dried (sodium sulfate) which
  6. customgave a yellow to green solution
  7. customEvaporation
  8. customgave a syrup which
  9. customwas chromatographed (SiO2, ethyl acetate:isooctane 2:1)

出典と根拠

ORDレコード
ord-36df67bfbe55479ca97689c189ee47e3
出典データセット
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04675392

反応ノート

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