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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644971Generated: October 29, 2026

Benzyl chloroformate → HCID 59263886, compound

https://huagongshe.com/reaction/644971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl N-(2-oxoethyl)carbamateHCID 4247255—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant7-(2-Aminoethyl)-4-hydroxy-1,3-benzothiazol-2(3H)-one hydrobromideHCID 13814270—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59263886HCID 59263886—

Reaction Steps

7-(2-Aminoethyl)-4-hydroxy-1,3-benzothiazol-2(3H)-one hydrobromide (3.66 g) was suspended in a mixture of THF (50 ml) and water (25 ml). Sodium hydrogen carbonate (1.06 g) was added and the mixture stirred for 15 min. Acetic acid (1.44 ml) was added, followed by a solution of tert-butyl (2-oxoethyl)carbamate (2.0 g) in THF (10 ml), and the mixture stirred for a further 30 min. Sodium cyanoborohydride (1.58 g) was added and the solution stirred for a further 18 h. Ethyl acetate (100 ml) and a solution of sodium hydrogen carbonate (3.17 g) in water (50 ml) were added, the mixture was stirred vigorously, benzyl chloroformate (709 ul) was added, and the mixture stirred for 15 min. A second portion of benzyl chloroformate (170 ul) was added and the mixture stirred for a further 30 min. The reaction mixture was extracted with ethyl acetate (×2) and filtered through celite. The organic extracts were combined, washed with water, dried (anhydrous Na2SO4), filtered and evaporated. The resulting material was purified by flash chromatography on silica using isohexane:ethyl acetate (50:50, 25:75, 100%) as eluent to give the sub-title compound (2.94 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700782B2
Source datasetuspto-grants-2010_04
ORD IDord-f581b5316d814a72bc3887d977216bb3
Source noteuspto-grants-2010_04