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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072870Generated: October 30, 2026

Hydrochloric Acid → ethyl 4-(N-benzyl-N-methylcarbamoyloxy)-2-butynoate

https://huagongshe.com/reaction/2072870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-MethylbenzylamineHCID 7669—
ReactantEthyl 4-(chlorocarbonyloxy)-2-butynoateHCID 14567687—
SolventDichloromethaneHCID 6344—
Productethyl 4-(N-benzyl-N-methylcarbamoyloxy)-2-butynoateHCID 1456768028.6%

Reaction Steps

2.85 g (15 millimoles) of ethyl 4-(chlorocarbonyloxy)-2-butynoate obtained in the first step of Example VI-9 was dissolved in 20 ml of dichloromethane, and 9 ml of a dichloromethane solution containing 3.1 ml (24 millimoles) of N-methylbenzylamine was rapidly added under cooling with ice. The mixture was reacted for 1 hour under stirring and cooling with ice. The reaction mixture was poured into ice water, adjusted to pH 2 with dilute hydrochloride acid and subjected to extraction treatment. The dichloromethane extraction solution was dried over sodium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (with use of 30 g of silica gel). The desired fraction eluted by hexane-benzene (1:0→3:1), was collected and concentrated under reduced pressure, whereby 1.18 g (yield: 28.5%) of colorless oily ethyl 4-(N-benzyl-N-methylcarbamoyloxy)-2-butynoate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914227
Source datasetuspto-grants-1990_04
ORD IDord-bdbc34154dc040f6b90bd197b94d8b33
Source noteuspto-grants-1990_04