HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285340Generated: October 30, 2026
Sodium Bicarbonate → 2-Cyano 3-(2,6-dichlorophenyl)propanoic acid
https://huagongshe.com/reaction/1285340
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Cyano-3-(2,6-dichlorophenyl)acrylic acid | HCID 54513790 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Cyano 3-(2,6-dichlorophenyl)propanoic acid | HCID 13560717 | 88.8% |
Reaction Steps
92 g of 2-cyano 3-(2,6-dichlorophenyl)propenoic acid (Tetrahedron Lett., 1975, p.3643-4) are put into 860 ml of methanol and 285 ml of a 10% sodium hydrogen carbonate solution. This is cooled to 18° C. and the necessary quantity of sodium borohydride is introduced over a two and one-half hour period. The mixture is left for 2 hours at ambient temperature, then concentrated and acidified by adding 1N hydrochloric acid until a pH of 2.3. The solution is then extracted with ether and the organic layer is washed with water, dried on magnesium sulphate, filtered and evaporated. 82.4 g of 2-cyano 3-(2,6-dichlorophenyl)propanoic acid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04567181 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-0089e5f64709483cba3b68bc71463bca |
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| Source note | uspto-grants-1986_01 |
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