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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872329Generated: November 2, 2026

1-Bromopropane → HCID 13871882, compound

https://huagongshe.com/reaction/1872329

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopropaneHCID 7840—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 4-chloroformylbutyrateHCID 73916—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13871882HCID 13871882—

Reaction Steps

2.82 g of magnesium is introduced into a 250 ml reaction vessel under a nitrogen atmosphere. It is covered with THF and 1 ml of 1-bromopropane is poured in. When the reaction starts, a solution of 9.9 ml of 1-bromopropane in 150 ml of THF is added dropwise over 1.5 hours. Once addition is complete, agitation is carried out for 10 minutes, then the reaction medium is taken to reflux for 3 hours followed by bringing to a temperature of -80° C. A solution of 17 ml of methyl 4-(chloroformyl)butyrate is added very slowly over 45 minutes. Agitation is then carried out for 1 hour at -70° C., then the reaction medium is allowed to return very slowly to 18° C. (over 17 hours). The reaction medium is treated by adding 160 ml of a saturated aqueous solution of ammonium chloride. Agitation is carried out for 30 minutes followed by decanting and re-extraction of the aqueous phase with 100 ml of ether. The organic phases are concentrated. The residue is taken up in 200 ml of ether, then washed twice with 100 ml of water followed by drying over magnesium sulphate and concentration with a rotary evaporator. In this way, 20.2 g of an oil corresponding to the expected product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107495
Source datasetuspto-grants-2000_08
ORD IDord-2a4af95130d242d69db43e23734c3703
Source noteuspto-grants-2000_08