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Methylamine → 1-(4-Bromophenyl)-2-methylaminoethanol

HRID 45516
Notes
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Reaction equation

HRID 45516 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:10][O:9]2)=[CH:4][CH:3]=1.[CH3:11][NH2:12]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([OH:9])[CH2:10][NH:12][CH3:11])=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6329MethylamineHCID 1194602-(4-Bromophenyl)oxirane

Product 1

HCID 219434331-(4-Bromophenyl)-2-methylaminoethanol

Procedure

A solution of 2-(4-bromophenyl)-oxirane (0.5 g, 2.51 mmol) in methylamine (6.6 ml, 33% by volume in ethanol, 25.12 mmol) was stirred at room temperature under an atmosphere of nitrogen. After 18 hours the solvent was removed in vacuo and the residue was purified over flash silica eluting with dichloromethane:methanol:acetic acid:water (120:15:3:2) to afford the desired compound as the acetic acid salt. Further purification over a Phenomenex_Strata_SCX column eluting with methanol followed by 2N ammonia in methanol gave the desired product. LC/MS: (PS-B3) Rt 2.52 [M+H]+ 230.

Workup

  1. customAfter 18 hours the solvent was removed in vacuo
  2. customthe residue was purified over flash silica eluting with dichloromethane:methanol:acetic acid:water (120:15:3:2)
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Sources & evidence

ORD record
ord-31b8b9c70e394d57831f1d439565f5fd
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08541461B2

Reaction notes

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