HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 23467854, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23467856 | HCID 23467856 | — |
| Product | HCID 23467854 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260761 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-1efb82ef0e804d779bde1adb35728fc7 |
| Source note | uspto-grants-1981_04 |