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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553629Generated: October 31, 2026

Boron tribromide → HCID 59267961, compound

https://huagongshe.com/reaction/553629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 59267860HCID 59267860—
SolventDichloromethaneHCID 6344—
ProductHCID 59267961HCID 59267961101.3%

Reaction Steps

To a solution of 5-(2-benzyloxy-1,1-dimethyl-ethyl)-1,3,4-thiadiazol-2-ylamine (15.0 g, 57.0 mmol) in DCM (100 mL), boron tribromide (1N in DCM, 15.0 mL, 162.0 mmol) is added slowly at 0° C. The reaction mixture is warmed up to room temperature and stirred for 3 h. After cooling the reaction mixture to 0° C., ice water is added. The two phases are separated and the pH of the water phase is adjusted to ˜13 with NaOH and extracted with n-BuOH. The organic layer is washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to afford 10.0 g of 2-(5-amino-1,3,4-thiadiazol-2-yl)-2-methyl-propan-1-ol as a brown solid; m/z 174 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048899B2
Source datasetuspto-grants-2011_11
ORD IDord-7b7d163e4f6c4935ba0fb21af6982cd1
Source noteuspto-grants-2011_11