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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341773Generated: October 30, 2026

Acetic Anhydride → HCID 53886620, compound

https://huagongshe.com/reaction/341773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 15136239HCID 15136239—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 53886620HCID 5388662097%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice-cooled solution of 4.13 g (20.7 mmol) 3-hydroxymethyl-2,5-dihydro-pyrrole-1-carboxylic acid tert-butylester and 244 mg (2 mmol) DMAP in 50 ml pyridine was added 3.06 g (30 mmol) acetic anhydride. The mixture was stirred for 30 min at 0° C., then for additional 60 min at room temperature. The mixture was poured on ice and extracted twice with ether. The combined organic layers were evaporated in vacuo, dissolved in ether, washed with sat. CuSO4, water and brine and dried over MgSO4. Evaporation and bulb-to-bulb distillation gave 4.82 g (97%) 3-acetoxymethyl-2,5-dihydro-pyrrole-1-carboxylic acid tert.-butylester as a colorless oil, b.p. 105° C. (0.2 mbar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856309
Source datasetuspto-grants-1999_01
ORD IDord-79f277808f6340488aeec1ea0cba696e
Source noteuspto-grants-1999_01