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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476350Generated: October 27, 2026

Methanesulfonic Acid → HCID 86657361, compound

https://huagongshe.com/reaction/476350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantL-Glutamic acid alpha-benzyl esterHCID 7009632—
Reactant16-(Benzyloxy)-16-oxohexadecanoic acidHCID 54271345—
SolventAcetoneHCID 180—
ProductHCID 86657361HCID 86657361—

Reaction Conditions

Temperature35 °C

Reaction Steps

1,16-hexadecanedioic acid mono benzyl ester (20.0 g, 53.1 mmol) was dissolved in acetone at 35-40° C. N-Hydroxysuccinimide (6.42 g, 55.8 mmol) was added. To the resulting solution dicyclohexylcarbodiimide (DCC) (12.1 g, 58.4 mmol) was added. The reaction mixture was stirred for 3-4 hours at 35° C. To the resulting suspension triethylamine (7.40 ml, 53.1 mmol) and L-glutamic acid α-benzyl ester (12.6 g/53.1 mmol) were added. The reaction mixture was stirred for 8-16 hours at 35-40° C. The reaction mixture was cooled to 20-25° C. Methanesulfonic acid (3.45 ml, 53.1 mmol) and DCC (12.1 g, 53.1 mmol) were added. The reaction mixture was stirred for 8-16 hours at 20-25° C. The reaction mixture was filtered, and the filtrate evacuated to dryness. The residue was partitioned between water (100 ml) and toluene (200 ml). The toluene phase was dried by distilling off water. Silica gel (20 g) was added to the residue. The suspension was stirred for 30 minutes at 20-25° C., subsequently filtered. The volume of the filtrate was reduced to app. 100-120 ml by evaporation under reduced pressure. N-heptane (150 ml) was added over a period of 15-30 minutes. The resulting suspension was stirred for 2 hours. The product was isolated by filtration, and dried to constant weight under reduced pressure at 20-25° C. Yield 21 g (58%) of white material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637647B2
Source datasetuspto-grants-2014_01
ORD IDord-0de47a50efbb4025953c6000339ee703
Source noteuspto-grants-2014_01