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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591069Generated: October 28, 2026

Pentane → methyl 2-[4-(3,4-dihydro-2H-1-benzopyran-6-yl)-2,5-dimethylthiophen-3-yl]-4,4-dimethylpentanoate

https://huagongshe.com/reaction/591069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
Reactantmethyl 2-[4-(3,4-dihydro-2H-1-benzopyran-6-yl)-2,5-dimethylthiophen-3-yl]prop-2-enoateHCID 86717848—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Productmethyl 2-[4-(3,4-dihydro-2H-1-benzopyran-6-yl)-2,5-dimethylthiophen-3-yl]-4,4-dimethylpentanoateHCID 7085542376%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under a nitrogen atmosphere, a solution of methyl 2-[4-(3,4-dihydro-2H-1-benzopyran-6-yl)-2,5-dimethylthiophen-3-yl]prop-2-enoate (42c) (114 mg, 0.35 mmol) in anhydrous tetrahydrofuran (5 mL) was cooled to −78° C. tert-Butyllithium 1.6M in pentane (0.24 mL, 0.38 mmol) was added dropwise and the reaction mixture was stirred at −78° C. for 20 minutes before being quenched with brine (3 mL). The mixture was extracted with dichloromethane (2×6 mL). The organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by preparative TLC (cyclohexane/ethyl acetate 70/30) to provide the desired product (42d) (102 mg, 0.26 mmol, 76%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-29878a34143b4866ad363c2cf895076e
Source noteuspto-grants-2016_01