Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261453Generated: November 2, 2026

Bromoacetic Acid → HCID 67415695, compound

https://huagongshe.com/reaction/2261453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetic AcidHCID 6227—
ReactantHCID 59593550HCID 59593550—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
ProductHCID 67415695HCID 6741569514.7%

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 (350 mg, 0.988 mmol, Intermediate 10) in isopropanol (5 mL) and 3 N aq. NaOH (1.5 mL) is treated with bromoacetic acid (274 mg, 1.98 mmol). The dark red reaction mixture is stirred at 70° C. After 1, 2, 3 and 18 h an additional portion of bromoacetic acid (274 mg, 1.98 mmol) and 3N aq. NaOH (1.5 mL) is added and stirring is continued for 2 h after the last addition. The reaction mixture is diluted with EA, and washed with 1 N aq. HCl. The aq. phase is extracted with EA. The combined organic extracts are dried over MgSO4 and evaporated. The crude product is purified by chromatography on prep. TLC plates with DCM containing 10% of methanol to give {2,6-dimethyl-4-[3-oxo-3-((1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propyl]-phenoxy}-acetic acid (60 mg) as a pale yellow oil; LC-MS: tR=1.07 min, [M+1]+=413.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846964B2
Source datasetuspto-grants-2010_12
ORD IDord-d5d2a3cf9c7a457798d0acde9290f325
Source noteuspto-grants-2010_12