Hydrochloric Acid → HCID 19855485, compound

HRID 1649943Notes

Reaction equation

HRID 1649943 reaction equation
[NH2:1][CH:2]1[CH2:11][CH2:10][C:9]2[C:8]([O:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:7][CH:6]=[CH:5][C:4]=2[CH2:3]1.[C:17]1([S:23](Cl)(=[O:25])=[O:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.[OH-].[Na+].Cl>>[C:17]1([S:23]([NH:1][CH:2]2[CH2:11][CH2:10][C:9]3[C:8]([O:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:7][CH:6]=[CH:5][C:4]=3[CH2:3]2)(=[O:25])=[O:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

5

Procedure

10 mmol of 6-amino-5,6,7,8-tetrahydro-naphth-1-yl-oxyacetic acid and 20 mmol of benzenesulphonyl chloride are warmed at 80° C. in 40 ml of 10% strength NaOH for 2 hours. The mixture is then acidified with concentrated HCl and the milky suspension is extracted by shaking twice with ethyl acetate. The combined ethyl acetate phases are rapidly extracted by shaking with 10% strength NaOH (product precipitates out of the ethyl acetate), the NaOH phase is acidified with concentrated HCl and extracted by shaking twice with ethyl acetate and the extract is dried over Na2SO4 and evaporated. The residue is boiled up in ethyl acetate and the mixture is filtered. The product crystallizes out after 2-3 hours in a refrigerator.

Workup

  1. extractionthe milky suspension is extracted
  2. extractionThe combined ethyl acetate phases are rapidly extracted
  3. stirringby shaking with 10% strength NaOH (product
  4. customprecipitates out of the ethyl acetate), the NaOH phase
  5. extractionextracted
  6. stirringby shaking twice with ethyl acetate
  7. dry with materialthe extract is dried over Na2SO4
  8. customevaporated
  9. filtrationthe mixture is filtered
  10. customThe product crystallizes out after 2-3 hours in a refrigerator

Sources & evidence

ORD record
ord-e58b00c2a52344b7bb3d9f15087a319d
Source dataset
uspto-grants-1990_05
Patent number
US04921998

Reaction notes

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