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Methanol → HCID 136354592, compound

HRID 1438695
Notes
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Reaction equation

HRID 1438695 reaction equation
OC1[C:3]2[CH:14]=[CH:13][CH:12]=[CH:11][C:4]=2[S:5][C:6]=1[C:7](=[NH:10])OC.[CH3:15][OH:16].[CH:17]([OH:20])([CH3:19])[CH3:18]>>[OH:16][C:15]1[C:3]2[CH:14]=[CH:13][CH:12]=[CH:11][C:4]=2[S:5][C:6]=1[C:7](=[NH:10])[O:20][CH:17]([CH3:19])[CH3:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 887MethanolHCID 3776IsopropanolHCID 3040798Benzo(b)thiophene-2-carboximidic acid, 3-hydroxy-, methyl ester

Product 1

HCID 136354592HCID 136354592, compound

Procedure

20 g of methyl 3-hydroxy-benzo[b] thiophene-2-carboximidate (Example 1) are heated under reflux in 500 ml of isopropanol for three days. The methanol being formed is constantly distilled off by passing through a stream of nitrogen. Evaporation to dryness and recrystallization of the residue from ethyl acetate yields yellow crystals with an m.p. of 208° C.

Workup

  1. distillationis constantly distilled off
  2. customEvaporation
  3. customto dryness and recrystallization of the residue from ethyl acetate
  4. customyields yellow crystals with an m.p. of 208° C.

Sources & evidence

ORD record
ord-aa17a417dc48429283d11be6c1334e15
Source dataset
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04056526

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes