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

Water → 5,6,7,8-tetrahydro-4H-thieno[2,3-c]azepine

HRID 2294843
Notes
Print preview

Reaction equation

HRID 2294843 reaction equation
[S:1]1[C:5]2[C:6](=O)[NH:7][CH2:8][CH2:9][CH2:10][C:4]=2[CH:3]=[CH:2]1.[BH4-].[Na+].O>O1CCCC1>[S:1]1[C:5]2[CH2:6][NH:7][CH2:8][CH2:9][CH2:10][C:4]=2[CH:3]=[CH:2]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 21471822HCID 21471822, compound

Product 1

HCID 214718605,6,7,8-tetrahydro-4H-thieno[2,3-c]azepineYield 66.8%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a mixture of 6.7 g of 4,5,6,7-tetrahydro-8H-thieno[2,3-c]azepin-8-one and 4.5 g of sodium borohydride in 70 ml of tetrahydrofuran was added boron trifluoride-ether complex dropwise under ice-cooling and the mixture was refluxed under heating for an hour. The mixture was poured into water, washed with chloroform, made alkaline with 10% potassium hydroxide solution and extracted with chloroform. The extract was washed with water, dried and concentrated to give 4.1 g of 5,6,7,8-tetrahydro-4H-thieno[2,3-c]azepine as an oil.

Workup

  1. additionwas added boron trifluoride-ether complex dropwise under ice-
  2. temperaturecooling
  3. temperaturethe mixture was refluxed
  4. temperatureunder heating for an hour
  5. washwashed with chloroform
  6. extractionextracted with chloroform
  7. washThe extract was washed with water
  8. customdried
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-95c0a80c49164f278985644451aa5c2f
Source dataset
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05691330

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes