Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223756Generated: October 31, 2026

Ethyl Acetate → HCID 23093714, compound

https://huagongshe.com/reaction/2223756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 23093710HCID 23093710—
SolventWaterHCID 962—
ProductHCID 23093714HCID 23093714—

Reaction Conditions

Temperature40 °C

Reaction Steps

3,4-Diethoxy-2-fluoro-6-formylbenzonitrile (5.90 kg, 24.87 mol) and ethyl acetate (59.0 L) were transferred to a reaction vessel under a nitrogen atmosphere, and while stirring, sodium triacetoxyborohydride (NaB(OAc)3H) (11.70 kg) was added. After 30 minutes of stirring, the internal temperature was heated up to 40° C., and the reaction solution was stirred for another 2 hours. The reaction solution was cooled, and at 15° C. internal temperature, water (2 L) was slowly added in drops, and excess sodium triacetoxyborohydride was degraded. Then more water (27.5 L) was added. The insoluble material was dissolved by increasing the outer bath temperature to 40° C., and the solution was separated after cooling. Following separation, the obtained organic layer was washed twice with an aqueous sodium bicarbonate solution and then with brine. The obtained organic layer was cooled in a 10° C. outer bath, and left to stand overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375236B2
Source datasetuspto-grants-2008_05
ORD IDord-c0aed101b17c47709dc5575fd6ec424b
Source noteuspto-grants-2008_05