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Cesium carbonate → HCID 54096342、化合物

HRID 1608093
ノート
印刷プレビュー

反応式

HRID 1608093 の反応式
[C:1]([O:4][C@@H:5]1[C@@H:32]([O:33][C:34](=[O:36])[CH3:35])[C@H:31]([O:37][C:38](=[O:40])[CH3:39])[C@@H:30]([CH2:41][O:42][C:43](=[O:45])[CH3:44])[O:29][C@H:6]1[O:7][CH2:8][CH2:9][S:10]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])(=O)=O)(=[O:3])[CH3:2].C(O[C@@H]1[C@@H](OC(=O)C)[C@H](OC(=O)C)[C@@H](COC(=O)C)O[C@H]1OCCBr)(=O)C.C(S)CCCCCCCCCCCCCCC.C(=O)([O-])[O-].[Cs+].[Cs+]>CCCCCC.C(OC(=O)C)C.O.ClCCl.CN(C)C=O>[C:1]([O:4][C@@H:5]1[C@@H:32]([O:33][C:34](=[O:36])[CH3:35])[C@H:31]([O:37][C:38](=[O:40])[CH3:39])[C@@H:30]([CH2:41][O:42][C:43](=[O:45])[CH3:44])[O:29][C@H:6]1[O:7][CH2:8][CH2:9][S:10][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])(=[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

10

反応物 4

HCID 10796Cesium carbonateHCID 18015HexadecanethiolHCID 106236332-Bromoethyl 2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosideHCID 56633597HCID 56633597、化合物

生成物 1

HCID 54096342HCID 54096342、化合物収率 64%

試薬・触媒・溶媒 5

HCID 962
Water
溶媒
HCID 6228Dimethylformamide溶媒
HCID 6344Dichloromethane溶媒
HCID 8058Hexane溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

2-(Hexadecylsulfonyl)ethyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside. 2-Bromoethyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside (Dahmen et al. Carbohydr. Res., 116 (1983)) (540 mg, 1.19 mmol), hexadecanethiol (383 mg, 1.49 mmol), cesium carbonate (292 mg, 0.89 mmol) and dimethylformamide (5 ml) was stirred overnight. Dichloromethane (75 ml) and water (40 ml) were added. The aqueous phase was extracted with dichloromethane (2×25 ml), the combined organic phases were dried (Na2SO4) and concentrated. Chromatography (SiO2 ; ethylacetate: hexane) gave pure 2-(hexadecylthio)ethyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside (480 mg, 0.76 mmol, 64%), which was dissolved in ethyl acetate (12 ml) and treated with m-chloroperbenzoic acid (1.71 mmol). After 4 hours the solvents were removed and the residue was dissolved in dichloromethane and filtered through alumina (10 g) to give the pure sulfone lipid (495 mg, 98%). [α]D23 =-8.7° (c=0.9 in CDCl3).

後処理

  1. extractionThe aqueous phase was extracted with dichloromethane (2×25 ml)
  2. dry with materialthe combined organic phases were dried (Na2SO4)
  3. concentrationconcentrated

出典と根拠

ORDレコード
ord-2cf32bcc55284b078af4869ffd7a4bc8
出典データセット
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04868289

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート