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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495341Generated: October 29, 2026

Oxalyl chloride → HCID 86584593, compound

https://huagongshe.com/reaction/495341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantPotassium bisulfateHCID 516920—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53249597HCID 53249597—
ProductHCID 86584593HCID 8658459355%

Reaction Steps

3.78 g (12.4 mmol) monomenthyl (−)-phthalate (Fluka) was heated at reflux in 19 ml oxalyl chloride (18 eq.) for 1.5 h. The excess oxalyl chloride was distilled under vacuum. 2.75 g crude acid chloride was then diluted in 5 ml THF cooled to −8° under argon, and 0.97 g (3 eq.) NaBH4 was added. The reaction mixture was maintained under stirring at 0° for 10 min and at ambient temperature for 30 min. The mixture was then poured over cold 5% KHSO4 then extracted using diethyl ether. Chromatography of the crude product over silica gel (93:7 toluene/ether) yielded 1.85 g (55%) pure (1R,3R,4S)-3-p-menthanyl 2-hydroxymethylbenzoate in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939835B2
Source datasetuspto-grants-2005_09
ORD IDord-d241bcd25d8149fc8072a5eb0b5367c5
Source noteuspto-grants-2005_09