Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sorbitol | HCID 5780 | — |
| Reactant | HCID 178484997 | HCID 178484997 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178485001 | HCID 178485001 | — |
Reaction Steps
474 parts of anhydrous sorbitol were melted in a stainless steel reactor equipped with agitation means and heated to a temperature of 105° C. The molten sorbitol was agitated at a speed of 100 r.p.m. to create a vortex and thereafter 25 parts of cimetidine (melting point 141°-143° C.) were added to the vortex slowly to avoid forming lumps. After complete addition, the melt was agitated for an additional 10 minutes. This melt was transferred to a Sigma blade mixer heated at 90° C. with hot water and agitated at 18 r.p.m. After 1 minute of mixing, 1% crystalline sorbitol seed fines (less than 325 mesh) were slowly added over the surface of the agitating melt to achieve a uniform dispersion of the seeds in the melt in order to initiate a rapid crystallization in the mixer. When the crystallizing mass achieved a dough-like consistency in the mixer, it was removed and placed on a tray, spread out and placed in an oven at 50° C. for 10 hours until it was fully crystallized. The crystalline mass was cooled and aggregates of the material were ground in a laboratory Waring blender (medium speed, 5 seconds), then screened to collect a -40/+100 mesh fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05075291 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-da296d10991d4262a9c782b1f25ed4ae |
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| Source note | uspto-grants-1991_12 |
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