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Acetic Acid → N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)benzene-1,2-diamine

HRID 1942157
Notes
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Reaction equation

HRID 1942157 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11]1[CH:20]=[CH:19][C:14]2[O:15][CH2:16][CH2:17][O:18][C:13]=2[CH:12]=1)([O-])=O.C(O)(=O)C.O>[Fe].C1(C)C=CC=CC=1>[O:15]1[CH2:16][CH2:17][O:18][C:13]2[CH:12]=[C:11]([NH:10][C:5]3[C:4]([NH2:1])=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH:20]=[CH:19][C:14]1=2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 176Acetic AcidHCID 962WaterHCID 9185966N-(2-nitrophenyl)-2,3-dihydrobenzo[b][1,4]dioxin-6-amine

Product 1

HCID 43148731N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)benzene-1,2-diamineYield 91.5%

Reagents, catalysts & solvents 2

HCID 23925IronCatalyst
HCID 1140
Toluene
Solvent

Procedure

A mixture of 6.3 g (23 mmol) of N-(2-nitrophenyl)-2,3-dihydrobenzo[b][1,4]dioxin-6-amine, 9.0 g (161 mmol) of iron powder, acetic acid (1 ml), water (35 ml) and toluene (70 ml) were heated to reflux for 8 hours. The reaction mixture was filtered aid to separate the waste. The organic layer of the filtrate was batched off, washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain 5.1 g (yield: 91%) of N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)benzene-1,2-diamine) as a brown liquid.

Workup

  1. temperaturewere heated
  2. temperatureto reflux for 8 hours
  3. filtrationThe reaction mixture was filtered aid
  4. customto separate the waste
  5. washwashed with water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-b7abcfb7ad7d44d792149595ac4d1643
Source dataset
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08389523B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes