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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762638Generated: November 1, 2026

(2-Phenoxy-5-thiazolyl)-methanol → 2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl) cyclopropane-carboxylic acid

https://huagongshe.com/reaction/1762638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Phenoxy-5-thiazolyl)-methanolHCID 13106154—
Reactant2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl) cyclopropane-carboxylic acidHCID 53915596—
Product2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl) cyclopropane-carboxylic acidHCID 53915596—
Product2,2-Dimethyl-3-(3-methoxy-3-oxo-1-propeny)-cyclopropane-carboxylateHCID 86743070—

Reaction Steps

Using the procedure of Example 9, the product of Step B and (1R, cis ΔZ) 2,2-dimethyl-3-(3-methoxy-3-oxo-1-propenyl)cyclopropane-carboxylic acid were reacted to obtain (2-phenoxy-5-thiazolyl)-methyl (1R, cis, ΔZ) 2,2-dimethyl-3-(3-methoxy-3-oxo-1-propenyl)-cyclopropane-carboxylate melting at 62° C. and havng a specific rotation of [α]D20 =+60.5°±1.5° (c=1.5% in benzene).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04833163
Source datasetuspto-grants-1989_05
ORD IDord-d364097e11a74c2a851cced8f410f150
Source noteuspto-grants-1989_05