Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664216Generated: October 31, 2026

Isopropyl chloroformate → HCID 67441573, compound

https://huagongshe.com/reaction/1664216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl chloroformateHCID 7917—
ReactantTriethylamineHCID 8471—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67440676HCID 67440676—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67441573HCID 67441573—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Benzyloxycarbonylamino-isophthalic acid monomethyl ester (10 g, 30.1 mmol, 1 eq) and Et3N (5 ml, 36.1 mmol, 1.2 eq) are suspended in a mixture of THF (200 ml) and N-methylpyrrolidone (200 ml). Isopropylchloroformate (42 ml, 1 N in toluene, 42 mmol, 1.4 eq) is added, and the reaction mixture is stirred for 30 min at 0° C. and then diluted with diethyl ether and water. The organic layer is washed with 0.1 N HCl and brine. NaBH4 (3.82 g, 101 mmol, 3.36 eq) is dissolved in H2O (100 ml), and the solution is added to the reaction mixture, which is then stirred for 1 h. Diethyl ether and H2O are added, and the organic layer is separated, washed with brine, dried over sodium sulfate, filtered and concentrated. The residue is purified by column chromatography using EtOAc/hexane in a ratio of 1 to 2 to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039455B2
Source datasetuspto-grants-2011_10
ORD IDord-eff0631a95594f8aa4816f5c2a162510
Source noteuspto-grants-2011_10