HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511709Generated: October 28, 2026
Sodium Iodide → 6-Hydroxyhexyl 3,5-dinitrobenzoate
https://huagongshe.com/reaction/511709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 3,5-Dinitrobenzoic acid | HCID 7433 | — |
| Reactant | 6-Chloro-1-hexanol | HCID 74828 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 6-Hydroxyhexyl 3,5-dinitrobenzoate | HCID 12995553 | 91% |
Reaction Steps
357.70 g (1.686 Mol) of 3,5-dinitrobenzoic acid is suspended in 750 ml of 1-methyl-2-pyrrolidone. The suspension is stirred up to 50° C. 386.36 g (4.599 Mol) of sodium hydrogen carbonate are added and the mixture is heated up to 90° C. 22.50 g (0.150 Mol) of sodium iodide and 204.0 ml (1.533 Mol) of 6-chlorohexanol are added to the reaction mixture which is heated to 100° C. for 1 h. After 1 h of reaction, the reaction is complete and the orange suspension is thrown on 2 l of ice and 1 l of water. The product is filtrated, washed water and dried at 50° C. under vacuum for 24 h to give 425.0 g (91%) of 6-hydroxyhexyl 3,5-dinitrobenzoate as a rose powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09097938B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-72b3247e66d848a196170708dc54c402 |
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| Source note | uspto-grants-2015_08 |
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