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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330370Generated: October 30, 2026

Tributylamine → HCID 15085414, compound

https://huagongshe.com/reaction/330370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
Reactant6-Amino-1-hexanolHCID 19960—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBiotinHCID 171548—
SolventDimethylformamideHCID 6228—
ProductHCID 15085414HCID 1508541495.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 10.0 g (41 mmoles) biotin (1) and 800 ml N,N-dimethylformamide was stirred until all of the biotin had dissolved. Then 12.8 ml (53.8 mmoles) of tributylamine was added and the solution stirred for 10 minutes. To this solution was added 6.4 ml (49.4 mmoles) of isobutyl chloroformate followed by stirring for 30 minutes. This solution was then slowly added to a cold (-5° C.) solution of 5.80 g (49.4 mmoles) 6-amino-1-hexanol in 800 ml N,N-dimethylformamide. Addition took place over a 30-minute period, and the temperature of the reaction mixture was maintained at 0° C. during the addition. After addition was complete, the reaction mixture was stirred at 0° C. for 3 hours, then allowed to warm to 20° C. The solution was evaporated under high vacuum (2 Torr) and the residue was dissolved in 400 ml of anhydrous ethanol with heating. The solution was stored at -20° C. overnight, filtered, and the white crystalline precipitate washed with anhydrous ethanol. The washed precipitate was allowed to air dry to yield 13.4 g of white crystals, with an Mp of 170°-176° C. Recrystallization from anhydrous ethanol yielded material of MP 179°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895955
Source datasetuspto-grants-1990_01
ORD IDord-5583c15c1e524f3db7bbd242686c2088
Source noteuspto-grants-1990_01