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

Stearic Acid → Azulenesulfonic acid

HRID 256300
Notes
Print preview

Reaction equation

HRID 256300 reaction equation
[C:1]1([S:11]([O-:14])(=[O:13])=[O:12])[C:10]2[C:4]([CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)=[CH:3][CH:2]=1.[Na+].C(O)(=O)CCCCCCCCCCCCCCCCC>>[C:1]1([S:11]([OH:14])(=[O:12])=[O:13])[C:10]2[C:4]([CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)=[CH:3][CH:2]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 5281Stearic AcidHCID 23702350HCID 23702350, compound

Product 1

HCID 9834293Azulenesulfonic acidYield 0%

Conditions

Temperature
80 °C

Procedure

Sodium azulenesulfonate (12 g), 186 g of hydroxypropylcellulose-M and 282 g of stearic acid were granulated by the same way as in Example 5. Each 160 mg of it was filled in a capsule No. 3. The capsules were placed in a fluidized bed granulator-drier, fluidized by heating with air (intake temperature: 80° C.) for 15 minutes, the heater was turned off and allowed to cool with air of the room temperature to give capsules each containing 4 mg of azulenesulfonic acid.

Workup

  1. addition
Each 160 mg of it was filled in a capsule No
  • temperatureto cool with air of the room temperature
  • Sources & evidence

    ORD record
    ord-d8bbaed987ed479a8c9abd44a4e1fad7
    Source dataset
    uspto-grants-1987_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04702918

    Reaction notes

    Loading…

    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes