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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280739Generated: October 29, 2026

Triethylamine → (RS)-2-(2-bromo-ethyl)-1,2,3,4-tetrahydro-naphthalen-2-ol

https://huagongshe.com/reaction/1280739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant(Rs)-2-(2-hydroxy-ethyl)-1,2,3,4-tetrahydro-naphthalen-2-olHCID 18425826—
SolventDichloromethaneHCID 6344—
Product(RS)-2-(2-bromo-ethyl)-1,2,3,4-tetrahydro-naphthalen-2-olHCID 1842578461%

Reaction Steps

To a 0° C. solution of triphenylphosphine (1.03 g, 3.93 mmol), in CH2Cl2 (15 ml) was added slowly a solution of bromine (0.192 ml, 3.74 mmol) in CH2Cl2. After 1 hour stirring at room temperature, the reaction mixture was cooled to 0° C. and treated slowly with a solution of (RS)-2-(2-hydroxy-ethyl)-1,2,3,4-tetrahydro-naphthalen-2-ol (0.72 g, 3.74 mmol) in CH2Cl2 (15 ml). After 1.5 hour stirring at room temperature, the reaction mixture was again cooled to 0° C., treated slowly with triethylamine (0.52 ml, 3.74 mmol), washed successively with H2O and brine, dried over Na2SO4, filtered and concentrated. The residue was chromatographed over silica gel (hexane-ethylacetate 9:1) to provide (RS)-2-(2-bromo-ethyl)-1,2,3,4-tetrahydro-naphthalen-2-ol (0.58 g, 61%) as a colorless oil, MS: m/e=255.1 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451819B2
Source datasetuspto-grants-2002_09
ORD IDord-e497cf153f0d4835a1ec64ec4bdca9a3
Source noteuspto-grants-2002_09