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Acetic Acid → 8-Aminodibenzo[b,f]thiepin-3-carboxylic Acid Hydrochloride Salt

HRID 1075003
Notes
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Reaction equation

HRID 1075003 reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]2[S:11][C:10]3[CH:12]=C(C#N)[CH:14]=[CH:15][C:9]=3[CH:8]=[CH:7][C:6]=2[CH:18]=1.[ClH:19].[C:20]([OH:23])(=[O:22])[CH3:21]>>[ClH:19].[NH2:1][C:2]1[CH:3]=[CH:4][C:5]2[S:11][C:10]3[CH:12]=[C:21]([C:20]([OH:23])=[O:22])[CH:14]=[CH:15][C:9]=3[CH:8]=[CH:7][C:6]=2[CH:18]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 131518838-Amino-3-cyanodibenzo[b,f]thiepin

Product 1

HCID 131518868-Aminodibenzo[b,f]thiepin-3-carboxylic Acid Hydrochloride Salt

Procedure

850 Mg. 8-amino-3-cyanodibenzo[b,f]-thiepin is refluxed in a mixture of 20 cc. acetic acid and 20 cc. concentrated hydrochloric acid for 48 hours. The suspended solid is filtered, washed with some acetic acid, dried overnight under vacuum at 70° C. to yield 600 mg. pure compound, m.p. 308°-311° C.

Workup

  1. filtrationThe suspended solid is filtered
  2. wash
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
washed with some acetic acid
  • customdried overnight under vacuum at 70° C.
  • customto yield 600 mg
  • Sources & evidence

    ORD record
    ord-87a8b10d034c4effae03c97243c04fde
    Source dataset
    uspto-grants-1983_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04394515

    Reaction notes

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