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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654626Generated: October 31, 2026

Potassium Hydroxide → HCID 21684200, compound

https://huagongshe.com/reaction/654626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantDiethyl 2-(3-methoxy-5-(methylthio)-4-propoxyphenyl)-2,5-dicyano-5-(3,4,5-trimethoxyphenyl)-1,6-hexanedioateHCID 15044973—
SolventEthanolHCID 702—
ProductHCID 21684200HCID 2168420066%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of diethyl 2-(3-methoxy-5-(methylthio)-4-propoxyphenyl)-2,5-dicyano-5-(3,4,5-trimethoxyphenyl)-1,6-hexanedioate (12.0 g, 0.019 mol) in ethanol (250 ml) was added potassium hydroxide (4.4 g, 0.079 mol). The reaction was heated to 95° C. for 20 minutes, then filtered, and the filtrate concentrated. Methanol (300 ml) was added to the residue, and the solution was stirred at room temperature overnight. The reaction was filtered and the precipitate dried to yield 2-(3-methoxy-5-methylthio)-4-propoxyphenyl)-5-(3,4,5-trimethoxyphenyl)-1,6-hexanedinitrile in a 66% yield. (m.p. 131°-132.5° C.). NMR (CDCl3): δ 1.04 (t, 3H, term CH3), 1.80 (m, 2H, OCH2CH2CH3), 2.18 (m, 2H, CH2 from ##STR30## 2.44 (m+s, SCH3 --CH2 from ##STR31## 3.90 (m, 14H, --OCH3 +OCH2CH2CH3), 6.64+6.72 (s, 2H, ArH), 6.71, 6.77, 6.81, 6.83 (d,d, 2H, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05132463
Source datasetuspto-grants-1992_07
ORD IDord-5c905bbaf6a54d20a0c31fa932f96650
Source noteuspto-grants-1992_07