Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167437Generated: October 31, 2026

2-((Tert-butoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid → HCID 58398107, compound

https://huagongshe.com/reaction/2167437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((Tert-butoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acidHCID 18988374—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 58398107HCID 5839810793%

Reaction Steps

To a solution of 0.245 mmol of 2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid in 2 ml dry THF were added at room temperature 0.736 mmol borane dimethyl sulphide complex and the mixture was stirred over night. The mixture was diluted with EtOAc and washed with saturated Na2CO3 solution and brine. The aqueous layer was extracted with EtOAc. The combined organic layers were washed, dried over MgSO4 and filtered. Evaporation of the solvent gave 60 mg of a pale yellow oil (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045459B2
Source datasetuspto-grants-2015_06
ORD IDord-67f4c24c680743a2ab5144a96680a492
Source noteuspto-grants-2015_06