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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2872Generated: October 25, 2026

Boron tribromide → (+/-)-trans-2-Diisopropylaminocarbonyl-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline hydrochloride

https://huagongshe.com/reaction/2872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantEther hydrochlorideHCID 10953452—
Reactant(+/-)-trans-2-diisopropylaminocarbonyl-6-ethyl-8a-(3-methoxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g] isoquinolineHCID 22883659—
SolventMethanolHCID 887—
Product(+/-)-trans-2-Diisopropylaminocarbonyl-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline hydrochlorideHCID 22883657—

Reaction Steps

1.0 g (2.2 mmol) of (±)-trans-2-diisopropylaminocarbonyl-6-ethyl-8a-(3-methoxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g] isoquinoline were treated with 1.15 ml (12.0 mmol) of boron tribromide as described in example 2. The crude product was dissolved in MeOH and the solution brought to acidic pH with HCl/Et2O . The solvent was evaporated in vacuo and the solid crystallized from acetone, yielding 0.5 g of the title compound. M.p.=263°-265° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731322
Source datasetuspto-grants-1998_03
ORD IDord-85e68abf33ca4928bc83045893ab7a1b
Source noteuspto-grants-1998_03