exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol manufacturers
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| | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol Basic information |
| Product Name: | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol | | Synonyms: | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol;tert-Butyl (1R,5S,6R)-6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate;(1R,5S,6r)-tert-Butyl 6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate;tert-butyl 6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate;exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methano;tert-Butyl (1S,5R)-6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate;3-Azabicyclo[3.1.0]hexane-3-carboxylic acid, 6-(hydroxymethyl)-, 1,1-dimethylethyl ester, (1α,5α,6α)-;(1R,5S,6r)-rel-3-Boc-6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane | | CAS: | 419572-18-2 | | MF: | C11H19NO3 | | MW: | 213.27 | | EINECS: | | | Product Categories: | | | Mol File: | 419572-18-2.mol | ![exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol Structure](CAS2/GIF/419572-18-2.gif) |
| | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol Chemical Properties |
| Boiling point | 308℃ | | density | 1.157 | | Fp | 140℃ | | storage temp. | 2-8°C | | pka | 14.94±0.10(Predicted) | | Appearance | Colorless to off-white Viscous Liquid | | InChI | InChI=1S/C11H19NO3/c1-11(2,3)15-10(14)12-4-7-8(5-12)9(7)6-13/h7-9,13H,4-6H2,1-3H3 | | InChIKey | JVIDPFGQYMFQDZ-UHFFFAOYSA-N | | SMILES | C12C(C1CO)CN(C(OC(C)(C)C)=O)C2 |
| | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol Usage And Synthesis |
| Uses | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol is a useful reactant in organic synthesis. | | Synthesis | The general procedure for the synthesis of tert-butyl rel-(1R,5S,6r)-6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate from di-tert-butyl dicarbonate and exo-3-azabicyclo[3.1.0]hexan-6-ylmethanol was as follows: (1R,5S,6R)-3-azabicyclo[3.1.0]hexan-6-ylmethanol (10 g. 88.4 mmol) was dissolved in a solvent mixture of dioxane and water (3:2, v/v), followed by addition of sodium hydroxide (4.2 g, 106 mmol) and di-tert-butyl dicarbonate (28.9 g, 132.6 mmol). After the reaction was carried out for 10 h, 50 mL of water was added to the reaction mixture. The reaction mixture was extracted with ethyl acetate (150 mL each time, 3 times). The organic phases were combined, washed with saturated sodium chloride solution (50 mL each time, 2 times), then dried with anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography using elution system C. The target product (1R,5S,6R)-tert-butyl 6-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate (16.9 g, 89.9% yield) was obtained as a pale yellow liquid. | | References | [1] Patent: US2014/336207, 2014, A1. Location in patent: Paragraph 0306; 0307
[2] Patent: EP2796460, 2014, A1. Location in patent: Paragraph 0181
[3] Patent: US2002/94989, 2002, A1
[4] Patent: US2006/47114, 2006, A1. Location in patent: Page/Page column 12-13
[5] Patent: US2006/229455, 2006, A1. Location in patent: Page/Page column 9 |
| | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-methanol Preparation Products And Raw materials |
| Raw materials | (1R,5S,6r)-3-tert-butyl 6-ethyl 3-azabicyclo[3.1.0]hexane-3,6-dicarboxylate-->(1α,5α,6α)-3-Azabicyclo[3.1.0]hexan-6-ylmethanol hydrochloride-->N-Boc-pyrroline-->CIVENTICHEM CV-4328-->ethyl 5-benzyl-1,3a,4,5,6,6a-hexahydro-4,6-dioxopyrrolo[3,4-c]pyrazole-3-carboxylate-->exo-3-Benzyl-3-azabicyclo[3.1.0]hexane-6-methanol-->(1R,5S,6R)-3-azabicyclo[3.1.0]hexan-6-ylmethanol-->triethyl(r)-cyclopropane-1,2,3-tricarboxylate-->1,2,3-cyclopropanetri-carboxylic acid-->3-Oxabicyclo[3.1.0]hexane-6-carboxylicacid,2,4-dioxo-,(1alpha,5alpha,6alpha)-(9CI)-->Di-tert-butyl dicarbonate | | Preparation Products | exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-carbaldehyde-->(1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid |
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