Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887007Generated: October 30, 2026

Dichloromethane ethylacetate → HCID 58114115, compound

https://huagongshe.com/reaction/1887007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantLithium diisopropylamineHCID 45051747—
ReactantHCID 178426069HCID 178426069—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58114115HCID 58114115—

Reaction Conditions

Temperature0 °C

Reaction Steps

(1S,6S)-4,6-Dimethyl-cyclohex-3-ene-carboxylic acid [5-(3,3-dimethyl-but-1-ynyl)-thiophen-3-yl]-(trans-4-hydroxy-cyclohexyl)-amide (1.74 g, 4.2 mmol) in THF (50 mL) was cooled to −78° C. and treated with lithium diisopropylamine (8.4 mL, 2.0M in heptane/THF/PhEt, 16.8 mmol) and allowed to warm to 0° C. over the course of 2 hours. CO2 was vigorously bubbled through the reaction solution for 10 minutes. The reaction was then quenched with the addition of iPrOH, diluted with ethyl acetate, washed with saturated NH4Cl(aq), dried over MgSO4, filtered, and concentrated. Silica gel chromatography (0-100% ethyl acetate/dichloromethane) afforded 530 mg (1.2 mmol) of the title compound: MS (m/z): 458.1 [M+H]+; HPLC retention time 4.35 min (2-98% acetonitrile: water with 0.05% trifluoroacetic acid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501714B2
Source datasetuspto-grants-2013_08
ORD IDord-36a4caa9428045f5a5e505f29db92de0
Source noteuspto-grants-2013_08