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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834797Generated: November 2, 2026

Triethylamine → HCID 20372098, compound

https://huagongshe.com/reaction/1834797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCarbonazidic acid, 1,1-dimethylethyl esterHCID 61256—
ReactantHCID 20372082HCID 20372082—
SolventDimethylformamideHCID 6228—
ProductHCID 20372098HCID 2037209865.6%

Reaction Conditions

Temperature35 °C

Reaction Steps

DL-α-Amino-(5,6-dihydro-1,4-oxathiin-2-yl)-acetic acid (25.4 g.) is suspended in dimethylformamide (435 cc.); tert.-butoxycarbonyl azide (41.5 g.) and triethylamine (51 cc.) are added. The reagents are left in contact for 48 hours whilst stirring at a temperature of 35° C. The solution is concentrated under reduced pressure (1 mm Hg), the residue is taken up in water (300 cc.), and the pH is adjusted to 8.5 by adding a saturated sodium bicarbonate solution. The aqueous phase is extracted twice with ethyl ether (a total of 500 cc.) which is discarded, and is then acidified to pH = 3 by adding 4 N hydrochloric acid A product precipitates, which is filtered off and then dissolved in methylene chloride (600 cc.). The solution obtained is dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (20 mm Hg). DL-α-Tert.-butoxycarbonylamino-(5,6-dihydro-1,4-oxathiin-2-yl)-acetic acid (26.2 g.), melting at 160° C is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071531
Source datasetuspto-grants-1978_01
ORD IDord-2dfa9a8e799c40358c70aceb19182541
Source noteuspto-grants-1978_01