Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298154Generated: October 29, 2026

Allyl bromide → 38434-35-4

https://huagongshe.com/reaction/2298154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant2-(2,3-Dihydro-1H-inden-1-yl)ethan-1-olHCID 12322863—
SolventAcetonitrileHCID 6342—
Product38434-35-4HCID 1232286891.7%

Reaction Steps

N,N-Carbonyl diimidazole (2.0 g, 12.3 mmol) was added to a solution of 2-indanylethanol (2.0 g, 12.3 mmol) in acetonitrile. The reaction mixture was stirred at room temperature for 1 h and allyl bromide (8.93 g, 73.8 mmol) was added. The reaction mixture was heated to 70° C. for 24 h and was poured onto water. The aqueous solution was extracted with Et2O and the organic solution was washed with water (1×) followed by brine (1×). The organic solution was dried over MgSO4, filtered, and concentrated to afford the title compound (2.54 g). 1H NMR (400 MHz, CDCl3) δ 7.10-7.25 (m, 4H), 3.48 (t, 2H), 3.11 (m, 2H), 2.63 (m, 3H), 2.07 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-b91c560948ca4dc9b4bf25c51bc1c34a
Source noteuspto-grants-2002_12