HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580936Generated: October 30, 2026
2-Chloro-4-nitrobenzoic acid → 2-(1,3-Dimethoxy-1,3-dioxopropan-2-yl)-4-nitrobenzoic acid
https://huagongshe.com/reaction/580936
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-4-nitrobenzoic acid | HCID 7448 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Product | 2-(1,3-Dimethoxy-1,3-dioxopropan-2-yl)-4-nitrobenzoic acid | HCID 10590078 | — |
Reaction Steps
A solution of 2-chloro-4-nitrobenzoic acid (75 g, 372 mmol) in dimethyl malonate (900 mL) was sparged with nitrogen for 15 min. Sodium methoxide (48.3 g, 894 mmol) was added in one portion and the contents exothermed to 480° C. Fifteen minutes later, copper (I) bromide (5.4 g, 37 mmol) was added in one portion and the contents heated to 70° C. for 24 hrs. The reaction was 70% complete by nmr, the contents heated to 85° C. for 6 hrs to completely consume the 2-chloro-4-nitrobenzoic. Water (900 mL) was added to the cooled reaction followed by hexanes (900 mL). The aqueous layer was separated, toluene (900 mL) added, filtered through celite, and aqueous layer separated. Fresh toluene (1800 mL) was added to the aqueous layer and the biphasic mixture acidified with 6N aqueous HCl (90 mL). A white precipitate formed and the contents stirred for 18 hrs. The product was filtered off and dried to give a white soid (78.1 g, 70%) mp=153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05919795 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-53ca45c7bf1f45ef8786d2aa0bee8b5b |
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| Source note | uspto-grants-1999_07 |
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