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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443571Generated: October 29, 2026

Allyl bromide → HCID 23467854, compound

https://huagongshe.com/reaction/443571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 23467856HCID 23467856—
ProductHCID 23467854HCID 23467854—

Reaction Steps

Thus, 9-methoxy-2,3,4,4a,5,6,7,7a-octahydro-1H-benzo[4,5]furo[3,2-e]isoquinoline, when treated with allyl bromide in the presence of a base such as potassium carbonate, gives 3-allyl-9-methoxy-2,3,4,4a,5,6,7,7a-octahydro-1H-benzo[4,5]furo[3,2-e]isoquinoline (R1 =CH2CH=CH2 ; R2 =MeO; R3, R4, R5 =H). Also, thienyl or furyl carbonyl chlorides followed by reduction with lithium aluminum hydride give 3-(2-thienylmethyl or 2-furylmethyl-9-methoxy-2,3,4,4a,5,6,7,7a-octahydro-1H-benzo[4,5]furo[3,2-e]isoquinoline ##STR81##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04260761
Source datasetuspto-grants-1981_04
ORD IDord-1efb82ef0e804d779bde1adb35728fc7
Source noteuspto-grants-1981_04