HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Water → HCID 11666911, compound

HRID 2061906
Notes
Print preview

Reaction equation

HRID 2061906 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH:10]=O)[C:6]=2[CH:12]=1.[S:13]([NH2:17])([NH2:16])(=[O:15])=[O:14].[BH4-].[Na+].O>C(O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[C:7]([CH2:10][NH:16][S:13]([NH2:17])(=[O:15])=[O:14])[C:6]=2[CH:12]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 82267SulfamideHCID 4311764Sodium borohydrideHCID 75374995-Bromo-1-benzothiophene-3-carbaldehyde

Product 1

HCID 11666911HCID 11666911, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

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. temperatureheated
  2. temperatureto reflux for three days
  3. extractionthe solution was extracted with chloroform (3×50 mL)
  4. concentrationThe extracts were concentrated
  5. filtrationfiltered

Sources & evidence

ORD record
ord-829ead83669e472299de5963e22d9e6a
Source dataset
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08283478B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes