HRID1792193

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：C1CCOC1.CCCC[N+](CCCC)(CCCC)CCCC.[F-]

HCID11078149

未命名化合物

结构：CCC(CC)(C/C=C/OC(C)(C)C1=CC[C@H]2C3=CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@]4(C)[C@H]3CC[C@]12C)O[Si](CC)(CC)CC

HCID86760151

未命名化合物

PRODUCTS

生成物

结构：CCC(O)(CC)C/C=C/OC(C)(C)C1=CC[C@H]2C3=CC=C4C[C@@H](O)C[C@H](O)[C@]4(C)[C@H]3CC[C@]12C

HCID86760152

未命名化合物

收率 100%

PROCEDURE

实验过程

1α,3β-Bis(tert-butyldimethylsilyloxy)-20-{4-ethyl-4-triethylsilyloxy-(2E)-hexenyloxy}-20-methylpregna-5,7,16-triene (350 mg, 0.430 mmol) and a 1M tetra-n-butylammonium fluoride tetrahydrofuran solution (15 ml) were subjected to reaction using a procedure similar to that of Example 5(2) (3 hours), worked up and purified by column chromatography (ethyl acetate) to give the titled compound (200 mg, 100%) as a yellow foam.

WORKUP

后处理

customof Example 5(2) (3 hours)
custompurified by column chromatography (ethyl acetate)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-53a60de633264b85b20c7661cfb5ed1c
来源数据集: uspto-grants-2006_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07074777B2
来源说明: uspto-grants-2006_07

反应 SMILES

[Si]([O:8][C@@H:9]1[C@@:45]2([CH3:46])[C:13](=[CH:14][CH:15]=[C:16]3[C@@H:44]2[CH2:43][CH2:42][C@@:41]2([CH3:47])[C@H:17]3[CH2:18][CH:19]=[C:20]2[C:21]([O:24]/[CH:25]=[CH:26]/[CH2:27][C:28]([CH2:39][CH3:40])([O:31][Si](CC)(CC)CC)[CH2:29][CH3:30])([CH3:23])[CH3:22])[CH2:12][C@@H:11]([O:48][Si](C(C)(C)C)(C)C)[CH2:10]1)(C(C)(C)C)(C)C.O1CCCC1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>>[CH2:29]([C:28]([OH:31])([CH2:39][CH3:40])[CH2:27]/[CH:26]=[CH:25]/[O:24][C:21]([CH3:23])([C:20]1[C@:41]2([CH3:47])[C@H:17]([C:16]3[C@H:44]([CH2:43][CH2:42]2)[C@:45]2([CH3:46])[C:13]([CH2:12][C@@H:11]([OH:48])[CH2:10][C@@H:9]2[OH:8])=[CH:14][CH:15]=3)[CH2:18][CH:19]=1)[CH3:22])[CH3:30]