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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259012Generated: October 29, 2026

Ethyl Acetate → HCID 12393690, compound

https://huagongshe.com/reaction/259012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12393665HCID 12393665—
SolventWaterHCID 962—
ProductHCID 12393690HCID 12393690—

Reaction Steps

To a solution of 1.0 g. of trans-2-amino-6-benzyloxy-1-hydroxy-5-methoxycarbonyl-1,2,3,4-tetrahydronaphthalene in 20 ml. of ethyl acetate are added 5 ml. of water and 400 mg. of ethyl chlorcarbonate, and with stirring at room temperature, 1.0 g. of anhydrous potassium carbonate is added in small portions. After one-hour stirring, the organic layer is recovered, washed with water, dried and concentrated under reduced pressure. The residue is recrystallized from ethyl acetate-n-hexane to obtain trans-6-benzyloxy-2-ethoxycarbonylamino-1-hydroxy-5-methoxycarbonyl-1,2,3,4-tetrahydronaphthalene as colorless needles melting at 147°-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035512
Source datasetuspto-grants-1977_07
ORD IDord-70108a1c59bf4136837270baf3a6ebad
Source noteuspto-grants-1977_07