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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613743Generated: October 31, 2026

Benzyl chloroformate → Benzyl (5-bromopyridin-2-yl)carbamate

https://huagongshe.com/reaction/613743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantDiisopropylethylamineHCID 81531—
SolventChloroformHCID 6212—
ProductBenzyl (5-bromopyridin-2-yl)carbamateHCID 10590824—

Reaction Steps

A solution of 2-amino-5-bromopyridine (6.92 g, 40 mmol) and 6.22 g (48 mmol) of diisopropylethylamine in 50 mL of chloroform was added dropwise to a solution of 8.19 g (48 mmol) of benzyl chloroformate in 20 mL of chloroform at about 0° C., with stirring. A voluminous white precipitate formed. After about 15 minutes, the mixture was filtered and the precipitate was washed three times with chloroform and dried to give 2.70 g of the title product, mp 184° C. (dec) (recrystallization solvent=2-propanol). 1H nmr (dimethylsulfoxide-d6): δ=10.48 (br s, 1 H), 8.37 (d, 1 H), 7.98 (d of d, 1 H), 7.81 (d, 1 H), 7.40 (m, 5 H), 5.17 (s, 2 H); ms (NH3Cl): m/z=307, 309 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008361
Source datasetuspto-grants-1999_12
ORD IDord-2331d59e7c71481d8c468f077dcd16ba
Source noteuspto-grants-1999_12