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Methane, dichloromethoxy- → 5-Bromo-1-benzothiophene-3-carbaldehyde

HRID 2061905
Notes
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Reaction equation

HRID 2061905 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[CH:7][C:6]=2[CH:10]=1.[CH3:11][O:12]C(Cl)Cl.C([O-])(O)=O.[Na+]>ClCCCl.[Ti](Cl)(Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH:11]=[O:12])[C:6]=2[CH:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 21004Methane, dichloromethoxy-HCID 516892Sodium BicarbonateHCID 27765785-Bromo-1-benzothiophene

Product 1

HCID 75374995-Bromo-1-benzothiophene-3-carbaldehydeYield 72.9%

Reagents, catalysts & solvents 2

HCID 24193Titanium TetrachlorideCatalyst
HCID 11
1,2-Dichloroethane
Solvent

Procedure

5-Bromobenzothiophene (1.60 g, 7.51 mmol) and dichloromethyl methyl ether (1.29 g, 11.3 mmol) were dissolved in anhydrous 1,2-dichloroethane (75 mL). Titanium tetrachloride (2.14 g, 11.3 mmol) was added, turning the solution dark. After one hour at room temperature, the reaction was poured into a mixture of saturated aqueous NaHCO3 and ice. The mixture was stirred for about 30 minutes and then was extracted with DCM (2×100 mL). The extracts were concentrated and chromatographed (0 to 5% ethyl acetate in hexane) to yield 5-bromo-benzo[b]thiophene-3-carbaldehyde (1.32 g). The 5-bromobenzothiophene-3-carboxaldehyde (1.20 g, 4.98 mmol) and sulfamide (4.0 g, 42 mmol) were combined in anhydrous ethanol (25 mL) and heated to reflux for three days. The reaction was cooled to room temperature and sodium borohydride (0.207 g, 5.47 mmol) was added. After five hours, water (50 ml) was added and the solution was extracted with chloroform (3×50 mL). The extracts were concentrated, suspended in a minimal amount of DCM, and filtered to provide the title compound as a yellow solid.

Workup

  1. extractionwas extracted with DCM (2×100 mL)
  2. concentrationThe extracts were concentrated
  3. customchromatographed (0 to 5% ethyl acetate in hexane)

Sources & evidence

ORD record
ord-09ba93cdb6484e54aa7d503ff3be9d13
Source dataset
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08283478B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes