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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261448Generated: November 4, 2026

2-Bromoethanol → HCID 11589375, compound

https://huagongshe.com/reaction/2261448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantHCID 59593550HCID 59593550—
SolventIsopropanolHCID 3776—
SolventSodium HydroxideHCID 14798—
ProductHCID 11589375HCID 1158937546.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-(3,5-dimethyl-4-hydroxy-phenyl)-1-((1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propan-1-one (3.00 g, 8.46 mmol, Intermediate 10) in isopropanol (80 mL) and 2 N aq. NaOH (30 mL) is treated with 2-bromoethanol (2.11 g, 16.9 mmol). The dark red reaction mixture is stirred at 70° C. for 5.5 h. The solvent is removed under reduced pressure and the residue is dissolved in EA and washed twice with water. The organic layer is dried over MgSO4 and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 1:1 to give 3-[4-(2-hydroxy-ethoxy)-3,5-dimethyl-phenyl]-1-((1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propan-1-one (1.57 g) as an orange oil; LC-MS: tR=1.09 min, [M+1]+=399.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846964B2
Source datasetuspto-grants-2010_12
ORD IDord-46e69f3634d04a1abc8ee2eab0f4de14
Source noteuspto-grants-2010_12