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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438727Generated: November 3, 2026

Diazomethane → HCID 13076873, compound

https://huagongshe.com/reaction/1438727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 12812406HCID 12812406—
SolventDiethyl EtherHCID 3283—
ProductHCID 13076873HCID 13076873—

Reaction Steps

To an ether solution of cis-6-chloro-4-phenyl-1,3-benzodioxan-2-carboxylic acid (2.14 g, 7.36 mmoles), chilled in an ice bath, was added an ethereal solution of diazomethane until the yellow color of the diazomethane was no longer discharged. The solution was stirred in the ice bath for 10 minutes at room temp. for 10 minutes, and finally at 35° for 15 minutes. The ether solution was washed with dil.NaHCO3 solution (2 portions), water (2 portions), and saturated brine (1 portion), and dried over anhydrous Na2SO4. The solvent was evaporated to yield a solid which was recrystallized from benzene-Skellysolve B (essentially n-hexane). The yield was 1.71 g (76%); m.p. 129.5°-131°. NMR (CDCl3), β6.6 (d, 1H, C(5)H, cis); 5.65 ppm (s, 1H, C(2)H, cis).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04056540
Source datasetuspto-grants-1977_11
ORD IDord-029b35d05f16401695956a36d38207da
Source noteuspto-grants-1977_11