HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9710Generated: October 28, 2026
Sodium Hydroxide → HCID 136663924, compound
https://huagongshe.com/reaction/9710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Olsalazine Dimethyl Ester | HCID 136454804 | — |
| Product | HCID 136663924 | HCID 136663924 | 65% |
Reaction Steps
To a solution of sodium hydroxide (48 g, 1.2 mol in 800 ml of water) was charged compound 1c (80 g, 0.24 mol) at 25–30° C. The resulting dark black-red coloured solution was heated to mild reflux (reaction mixture temperature ˜85–90° C.) and was held for 90 minutes. This was then treated with activated carbon and refluxed further for 30 minutes. Then the reaction mixture was cooled to 45–50° C. and was filtered through a celite bed (prepared in water). The celite bed was washed with water (4×80 ml) and was mixed with the main filtrate. Further 240 ml of water was added to the combined filtrate and washings and cooled to 25–30° C. with efficient stirring. The pH of this resulting solution was adjusted to 6.0±0.05 with dropwise addition of 20% v/v aqueous acetic acid over 30–45 minutes. The resulting yellow slurry was cooled to 0–5° C. and stirred for 30 minutes to complete the crystallization. Compound 1d thus obtained was filtered and washed with water (2×160 ml) followed by isopropanol wash (2×40 ml). The wet cake obtained (107 g) was dried at 70° C. under reduced pressure (˜650 mm of Hg) for 16 hours to constant weight. The title compound 1d was obtained in 65% yield (55 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091327B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-2635a3a0c47f4c8d9e9782d14c61bc34 |
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| Source note | uspto-grants-2006_08 |
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