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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203286Generated: October 31, 2026

Sodium Carbonate → HCID 86702445, compound

https://huagongshe.com/reaction/2203286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantEthyl chloroformateHCID 10928—
ReactantMethyl 3-amino-4-formylbenzoateHCID 18412577—
CatalystEthyl chloroformateHCID 10928—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86702445HCID 8670244541.4%

Reaction Steps

To a mixture of methyl 3-amino-4-formylbenzoate (110 mg, 0.614 mmol) in 6 mL THF plus 4 mL saturated NaHCO3 and 1 mL H2O at rt was added ethyl chloroformate (0.070 mL, 0.737 mmol) at the reaction stirred at rt. After 50 min, an additional 0.5 mL saturated NaHCO3 and 5 drops ethyl chloroformate was added. At 17.5 hours the mixture was heated to 60° C., 1 mL saturated Na2CO3 added, and 5 drops ethyl chloroformate added. Then to push reaction to completion, a small scoop of solid Na2CO3 was added and additional ethyl chloroformate added drop-wise until the reaction was approximately 80% complete (45 hours total reaction time). The reaction was partitioned between EtOAc and aqueous NaHCO3 solution, the EtOAc layer washed with brine, dried with Na2SO4, and evaporated. The solid was crystallized from hexane/EtOAc and the filtrate chromatographed eluting with 2.5% MeOH/CHCl3. The impure products from crystallization and chromatography were combined and then recrystallized from hexane/EtOAc to give the title compound as a light yellow solid (63.8 mg, 41%). 1H NMR (CDCl3) δ: 10.53 (br. s, 1H), 10.00 (d, J=0.6 Hz, 1H), 9.11-9.12 (m, 1H), 7.80-7.84 (m, 1H), 7.72-7.76 (m, 1H), 4.28 (q, J=7.2 Hz, 2H), 3.95 (s, 3H), 1.35 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365575B2
Source datasetuspto-grants-2016_06
ORD IDord-419bee72dbe54415ad2e609247ccc32d
Source noteuspto-grants-2016_06