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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413564Generated: November 1, 2026

Acetyl chloride → 2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol diacetate

https://huagongshe.com/reaction/2413564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTetrahydrofuranHCID 8028—
Reactant2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol hydrochlorideHCID 13375278—
Product2-((6-Chrysenylmethyl)amino)-2-methyl-1,3-propanediol diacetateHCID 1559931865.2%

Reaction Steps

A mixture of 2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol hydrochloride (1B, 5.0 g, 13.1 mmol) and acetylchloride (Aldrich, 5.0 mL, 70.3 mmol) was refluxed in dry THF (200 mL) under N2 for 12 h. The reaction mixture was poured into a satd. NaHCO3 solution (500 mL) and extracted with EtOAc (3×500 mL). The EtOAc layers were combined, dried (K2CO3) and filtered to give a slightly yellow liquid. The solvent was removed to give an off-white solid. This was recrystallized 3× from PhCH3 /hexane (1:1). After filtration and drying, 3.67 g (65.2%) of 2-((6-chrysenylmethyl)amino)-2-methyl-1,3-propanediol diacetate was obtained mp 136°-137.5°, (C, H, N).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719046
Source datasetuspto-grants-1988_01
ORD IDord-222d3c013d264cc38e6cb45122acae5e
Source noteuspto-grants-1988_01