HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847397Generated: October 29, 2026
Hydrochloric Acid → HCID 178526205, compound
https://huagongshe.com/reaction/847397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | HCID 178515948 | HCID 178515948 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178526205 | HCID 178526205 | 34.9% |
Reaction Steps
To a stirred suspension of 50.0 g (0.125 mol) diselenosalicylic acid in 380 ml water is added 38.0 g (0.95 mol) sodium hydroxide, when the internal temperature rises to 45° C. and the acid goes into solution. On addition of 100 g (0.94 mol) sodium carbonate and 58 g (0.33 mol) sodium dithionite the temperature increases to 55° C. The mixture is heated to reflux for 2 h, allowed to cool to room temperature and 47.6 ml (68.4 g; 0.4 mol) benzyl bromide is added dropwise within 10 minutes. Further water (100 ml) is added and the stirring is continued at room temperature for 14 hours, then 355 ml (32%) hydrochloric acid is slowly added to the reaction mixture with stirring, the precipitated white solid is filtered off and then washed to neutrality with water. The moist product is recrystallized from 1600 ml propanol with the addition of 3 g active charcoal. The yield is 48.8 g (67% of th.). The mother liquors yield a further 12 g (16.5%) 2-benzylselenobenzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05141955 |
|---|
| Source dataset | uspto-grants-1992_08 |
|---|
| ORD ID | ord-028fdae4d6a44b3ea82e6924c9afef3e |
|---|
| Source note | uspto-grants-1992_08 |
|---|