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HRID1715078

反应详情

EQUATION

反应方程式

HRID 1715078 的结构方程式

REACTANTS

反应物

2
结构：O=C(OCC1c2ccccc2-c2ccccc21)N1CC[C@H]2OC[C@H](O)[C@H]21
HCID59343384

未命名化合物

结构：CC(C)(C)OC(=O)N1CC[C@H]2OC[C@H](O)[C@H]21
HCID66986914

未命名化合物

PRODUCTS

生成物

1
结构：O[C@H]1CO[C@@H]2CCN[C@H]12
HCID55287552

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

2
结构：Cl
溶剂HCID313

Hydrochloric Acid

ClH

结构：C1COCCO1
溶剂HCID31275

1,4-Dioxane

C4H8O2

PROCEDURE

实验过程

Preparation of (3R,3aR,6aR)-(9H-fluoren-9-yl)methyl 3-hydroxytetrahydro-2H-furo[3,2-b]pyrrole-4(5H)-carboxylate (2b). Alcohol (2f) (558 mg, 2.43 mmol) was dissolved in 4M HCl in dioxane (14.06 mL) and left to stand at ambient temperature for 1 h. The solvent was removed in vacuo and the residue azeotroped from toluene (3×20 mL) to give hydrochloride salt of (3R,3aR,6aR)-hexahydro-2H-furo[3,2-b]pyrrol-3-ol (2 g) used directly in the following step.

WORKUP

后处理

  1. waitleft
  2. customThe solvent was removed in vacuo
  3. customthe residue azeotroped from toluene (3×20 mL)