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1,4-Dioxane hydrochloride → HCID 44818810, compound

HRID 1909635
Notes
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Reaction equation

HRID 1909635 reaction equation
C[O:2][C:3](=[O:28])[CH2:4][CH2:5][CH2:6][N:7]1[CH2:11][CH2:10][CH2:9][C@@H:8]1[CH2:12][O:13][C:14]1[CH:19]=[CH:18][C:17]([O:20][C:21]2[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=2)=[CH:16][CH:15]=1.Cl.O1CCOCC1>>[ClH:27].[Cl:27][C:24]1[CH:25]=[CH:26][C:21]([O:20][C:17]2[CH:18]=[CH:19][C:14]([O:13][CH2:12][C@H:8]3[CH2:9][CH2:10][CH2:11][N:7]3[CH2:6][CH2:5][CH2:4][C:3]([OH:28])=[O:2])=[CH:15][CH:16]=2)=[CH:22][CH:23]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 204431481,4-Dioxane hydrochlorideHCID 44819172HCID 44819172, compound

Product 1

HCID 44818810HCID 44818810, compoundYield 49.5%

Procedure

Following the general procedure for Example 18, the product from step 1 (0.80 g 1.99 mmol) was treated with a 1:1 mixture of concentrated HCl/dioxane (36 mL) to afford the title compound (0.21 g, 26%) as a white solid.

Sources & evidence

ORD record
ord-a8c7144870944941a72291a1907f9ade
Source dataset
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08598359B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes